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Pediatrics Podiatry Primary care General practice Public health Psychiatry Addiction medicine Radiology Recreation therapy Rehabilitation medicine Respiratory medicine Pulmonology Sleep medicine Rheumatology Sports medicine Surgery Bariatric surgery Cardiothoracic surgery Neurosurgery Plastic surgery Traumatology Urology Andrology Pharmaceutical sciences Pharmacy Behavioral medicine Clinical psychology Health psychology Medical psychology Counseling psychology Veterinary medicine Physical fitness Group Fitness / aerobics Personal fitness training Kinesiology / Exercise Science / Human Performance

A

Abortion - Accident - Activities of daily living - Acupuncture - Adolescent medicine - Adult daycare center - Advance health care directive - Aerobic exercise - Age-adjusted life expectancy - Ageless - Aging and memory - Aging - Alcoholism - Allergy - Alternative medicine - Amputation - Anaerobic exercise - Anaesthesia - Anatomical pathology - Anatomy - Andrology - Animal-assisted therapy - Antibiotic resistance - Appetite - Assisted reproductive technology - Athletic training - Audiology - Autoimmune disease - Auxology

B

Bacterium - Baldness - Basic life support - Binge eating - Biochemical pathology - Biological standard of living - Biomedical research - Biomedical technology - Bipolar disorder - Birth attendant - Birth control - Blood diseases - Blood test - Body composition - Body Mass Index (BMI) - Body shaping - Body treatment - Brain death

C

Cancer - Cell replacement therapy - Chemotherapy - Child birth - Chinese medicine - Chiropractic - Clinical death - Cognitive enhancement - Cognitive therapy - Collaborative therapy - Community-based rehabilitation - Community health - Complementary and alternative medicine - Complementary medicine - Convalescence - Cryosurgery

D

Death - Deficiency disease - Dental hygiene - Dentistry - Dermatology - Determinants of health - Detoxification - Developmental disability - Diabetes - Diagnosis - Diet (nutrition) - Diet and obesity - Dietary fiber - Dietary mineral - Dietary supplement - Dietetics - Dieting - Digestion - Digestive system - Digestive tract - Disability - Disease registry - Disease - Doctor-patient relationship - Dysarthria - Dyslexia

E

Ecological health - Energy medicine - Environmental health - Enzyme - Epidemic - Ethnicity and health - Evidence-based medicine - Evidence-based practice - Evolutionary medicine - Eugenics - Exercise equipment - Exercise physiology - Exercise

F

Fad diet - Faith healing - Family centered care - Family planning - Famine - Fast food - Female infertility - Fertility - Fetal alcohol syndrome - Folk medicine - Food additive - Food allergy - Food and cooking hygiene - Food groups - Food pyramid - Food quality - Food science - Food supplements - Food technology - Food - Forensic pathology - Free clinic - Functional diversity

G

Gene therapy - General fitness training - General surgery - Genetic counseling - Genetic engineering - Genetically modified organism - Genetics - Genital integrity - Genitourinary medicine - Genome project - Genome - Genomics - Geriatric sexology - Geriatrics - Gerontology - Gynaecology

H

Haematology - Hand surgery - Healer - Healing - Health applications and clinical studies of meditation - Health care delivery - Health care industry - Health care system - Health care - Health claims on food labels - Health disparities - Health economics - Health education - Health geography - Health literacy - Health observatory - Health profession - Health promotion - Health science - Health specialties - Health - Healthcare inequality - Healthcare - Healthy diet - Healthy eating - History of medicine - Holistic health - Home birth - Home remedy - Homeopathy - Homeostasis - Hormone - Hospice - Hospital accreditation - Hospital - Human anatomy - Human cloning - Human enhancement - Hygiene

I

Illness - Illnesses related to poor nutrition - Immortality - Immunity (medical) - Immunology - Infectious diseases - Infertility - Inflammation - Injury - Internal medicine

J

K

L

Life - Life expectancy - Life extension - Life span - Longevity

M

Macronutrient - Male infertility - Malnutrition - Manipulative therapy - Manual therapy - Maternal health - Maximum life span - Medical cannabis - Medical case management - Medical devices - Medical herbalism - Medical history - Medical imaging - Medical model - Medical physics - Medical privacy - Medical school - Medical sociology - Medical technology - Medical tourism - Medication - Medicine - Megadose - Megavitamin therapy - Men's health - Mental disorder - Mental health - Mental hygiene - Mental retardation - Metabolism - Meteoropathy - Microbiology - Micronutrient - Midwifery - Mind-body intervention - Miscarriage - Mortality rate - Multivitamin - Mutation

N

Nanomedicine - Nanotechnology - Natalism - Naturopathic medicine - Neuroimmunology - Neurology - Neuroscience - Neurosurgery - Noise health effects - Non-infectious disease - Nuclear medicine - Nurse - Nursing school - Nursing - Nutrient density - Nutrient - Nutrigenomics - Nutrition and pregnancy - Nutrition - Nutritional supplement - Nutritionist

O

Obesity - Obstetrics and gynaecology - Obstetrics - Occupational hygiene - Occupational medicine - Occupational safety and health - Occupational therapy - Old age - Oncology - Online pharmacy - Ophthalmology - Optometry - Oral hygiene - Organ transplant - Organic food - Organism - Orthopaedics - Osteopathy - Over-the-counter drug - Overweight

P

Palliative care - Paramedic - Pathogen - Pathology - Pediatrics - Perioperative medicine - Pharmaceutical care - Pharmaceutical policy - Pharmaceutical sciences - Pharmacology - Pharmacy - Physical education - Physical examination - Physical exercise - Physical fitness - Physical therapy - Physician - Plastic surgery - Population health - Positive mental attitude - Posture and occupational health - Pre-conception counseling - Pregnancy - Pregnant patients' rights - Prenatal care - Prescription drugs - Preventive medicine - Primary care - Primary health care - Psychiatry - Psychoanalysis - Psychoeducation - Psychoneuroimmunology - Psychotherapy - Public health

Q

Quality of Life (Healthcare)

R

Radiology - Rare disease - Rejuvenation (aging) - Reproductive endocrinology and infertility - Reproductive health - Reproductive medicine - Rheumatology - Rural health - Rural health clinic

S

STD testing - Safe sex - Sanitation - Saturated fat - Self care - Self-healing - Self-medication - Senility - Sex and illness - Sex education - Sexual dysfunction - Sexual health clinic - Sexual health - Sexuality and disability - Sexuality education - Sleep deprivation - Sleep hygiene - Sleep - Smoking cessation - Social determinants of health - Social medicine - Special needs - Sports medicine - Sports nutrition - Stem cell treatments - Stress (medicine) - Stress management - Supported living - Surgery - Survivability - Symptom

T

Therapy dog - Toxicity - Toxicology - Toxin - Traditional Chinese medicine - Traditional Korean medicine - Traditional medicine - Trans fat - Trauma surgery

U

Universal design

V

Vaccine - Vegetarianism - Virus - Vitamin - Vulvovaginal health

W

Weight loss - Wellness (alternative medicine) - Wellness - Witch-doctor - Women's health - Workplace health surveillance - Workplace wellness - World Health Organization

X

X-ray

Y

Z

See also

List of diseases

0-9

 

11 beta hydroxylase deficiency - 10q Partial trisomy, rare (NIH) [1] - 11 beta hydroxysteroid dehydrogenase type 2 deficiency - 17 alpha hydroxylase deficiency - 17 beta hydroxysteroide dehydrogenase deficiency - 17 Beta-hydroxysteroid dehydrogenase deficiency, rare (NIH) - 18-Hydroxylase deficiency, rare (NIH) - 18p syndrome, rare (NIH) - 1p36 Deletion Syndrome, rare (NIH) - 2-hydroxyethyl methacrylate sensitization, rare (NIH) - 2-hydroxyglutaricaciduria - 2-Hydroxyglutaricaciduria, rare (NIH) - 2-Methylacetoacetyl CoA thiolase deficiency, rare (NIH) - 2,8 dihydroxy-adenine urolithiasis - 21 hydroxylase deficiency - 22q11.2 deletion syndrome, rare (NIH) - 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency, rare (NIH) - 3 alpha methylcrotonyl-coa carboxylase 2 deficiency, rare (NIH) - 3 alpha methylglutaconic aciduria, type 3, rare (NIH) - 3 beta hydroxysteroid dehydrogenase deficiency - 3 hydroxyisobutyric aciduria - 3 methylcrotonic aciduria - 3 methylglutaconyl coa hydratase deficiency - 3-hydroxy 3-methyl glutaryl-coa lyase deficiency - 3-hydroxyacyl-coa dehydrogenase deficiency - 3-Hydroxyisobutyric aciduria, rare (NIH) - 3-methyl crotonyl-coa carboxylase deficiency - 3-methyl glutaconic aciduria - 3C syndrome, rare (NIH) - 3-M syndrome, rare (NIH) - 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, rare (NIH) - 4-hydroxyphenylacetic aciduria, rare (NIH), Optic atrophy, [1] - 46 xx gonadal dysgenesis epibulbar dermoid - 46,XX Gonadal dysgenesis epibulbar dermoid, rare (NIH) - 47 XXY syndrome - 47 xyy syndrome - 47 XYY syndrome, rare (NIH), see Klinefelter's syndrome - 47,XXX syndrome, rare (NIH) , see Klinefelter's syndrome - 48 xxxx syndrome - 48 xxyy syndrome - 49 xxxxx syndrome - 49 xxxxy syndrome - 49,XXXXX syndrome, rare (NIH) , see Klinefelter's syndrome - 49,XXXXY syndrome, rare (NIH) , see Klinefelter's syndrome - 5 alpha reductase 2 deficiency - 5-alpha-Oxoprolinase deficiency, rare (NIH) - 5-Nucleotidase syndrome, rare (NIH) - 5q-syndrome, rare (NIH) - 6 alpha mercaptopurine sensitivity, rare (NIH) - 6-pyruvoyl-tetrahydropterin synthase deficiency, rare (NIH) - 6-pyruvoyltetrahydropterin synthase deficiency - 7-dehydrocholesterol reductase deficiency -

 

 

Aa-Ab

Aagenaes syndrome - Aarskog Ose Pande syndrome - Aarskog syndrome - Aase Smith syndrome - Aase syndrome - ABCD syndrome - Abasia - Abdallat Davis Farrage syndrome - Abdominal aortic aneurysm - Abdominal cystic lymphangioma - Abdominal defects - Abdominal musculature absent microphthalmia joint laxity - Abdominal neoplasm / Abdominal neoplasms - Aberrant subclavian artery - Ablepharon macrostomia syndrome - Abnormal systemic venous return - Abruzzo Erickson syndrome - Absence of Gluteal muscle - Absence of tibia with polydactyly - Absent corpus callosum cataract immunodeficiency - Absent T lymphocytes -

Ac

Aca-Acc

Acalvaria - Acanthocheilonemiasis - Acanthocytosis chorea - Acanthocytosis - Acanthosis nigricans - Acatalasemia - Accessory deep peroneal nerve - Accessory Navicular bone - Accessory pancreas -

Ach-Ack

Achalasia alacrimia syndrome - Achalasia microcephaly - Achalasia, familial esophageal - Achalasia - Achalasia-Addisonianism-Alacrima syndrome - Achard syndrome - Achard-Thiers syndrome - Acheiropodia - Achondrogenesis Kozlowski type - Achondrogenesis type 1A - Achondrogenesis type 1B - Achondrogenesis type 2 - Achondrogenesis - Achondroplasia Swiss type agammaglobulinemia - Achondroplasia - Achondroplastic dwarfism - Achromatopsia incomplete, X-linked - Achromatopsia - Acid maltase deficiency - Acidemia, isovaleric - Acidemia, propionic - Acitretine antenatal infection - Ackerman syndrome -

Acn-Acq

Acne rosacea - Acne - Acoustic neuroma - Acoustic schwannomas - Acquired agranulocytosis - Acquired hypoprothrombinemia - Acquired Immune Deficiency Syndrome - Acquired ichthyosis - Acquired prothrombin deficiency - Acquired syphilis - anger irritation syndrome[ais] -

Acr

Acra

Acral dysostosis dyserythropoiesis - Acral renal mandibular syndrome -

Acro

Acro coxo mesomelic dysplasia - Acro fronto facio nasal dysostosis -

Acroc-Acrok

Acrocallosal syndrome, Schinzel type - Acrocephalopolydactyly - Acrocephalosyndactyly Jackson Weiss type - Acrocephaly - Acrocephaly pulmonary stenosis mental retardation - Acrocyanosis - Acrodermatitis enteropathica - Acrodermatitis - Acrodysostosis - Acrodysplasia - Acrodysplasia scoliosis - Acrofacial dysostosis - Acrofacial dysostosis ambiguous genitalia - Acrofacial dysostosis atypical postaxial - Acrofacial dysostosis Catania form - Acrofacial dysostosis Preis type - Acrofacial dysostosis Rodriguez type - Acrofacial dysostosis Weyers type - Acrofacial dysostosis, Nager type - Acrofacial dysostosis, Palagonia type - Acrokeratoelastoidosis of Costa -

Acrom-Acros

Acromegaloid changes cutis verticis gyrata corneal - Acromegaloid facial appearance syndrome - Acromegaloid hypertrichosis syndrome - Acromegaly - Acromesomelic dysplasia Brahimi Bacha type - Acromesomelic dysplasia Campailla Martinelli type - Acromesomelic dysplasia Hunter Thompson type - Acromesomelic dysplasia, Maroteaux type - Acromesomelic dysplasia - Acromicric dysplasia - Acroosteolysis dominant type - Acroosteolysis neurogenic - Acroosteolysis osteoporosis skull and mandible changes - Acropectoral syndrome - Acropectorenal field defect - Acropectorovertebral dysplasia - Acrophobia - Acropigmentation of Dohi - Acrorenal syndrome recessive - Acrorenoocular syndrome - Acrospiroma -

Act

ACTH deficiency - ACTH resistance - Atelectasis - Actinic keratosis - Actinomycetales causes anal infection - Actinomycosis - Activated protein C resistance -

Acu

Acut

Acuta

Acutane embryopathy -

Acute

Acute a-Acute l

Acute anxiety - Acute articular rheumatism - Acute erythroblastic leukemia - Acute febrile neutrophilic dermatosis - Acute gouty arthritis - Acute idiopathic polyneuritis - Acute intermittent porphyria - Acute lymphoblastic leukemia congenital sporadic aniridia - Acute lymphoblastic leukemia - Acute lymphocytic leukemia -

Acute m-Acute p

Acute megakaryoblastic leukemia - Acute monoblastic leukemia - Acute monocytic leukemia - Acute mountain sickness - Acute myeloblastic leukemia type 1 - Acute myeloblastic leukemia type 2 - Acute myeloblastic leukemia type 3 - Acute myeloblastic leukemia type 4 - Acute myeloblastic leukemia type 5 - Acute myeloblastic leukemia type 6 - Acute myeloblastic leukemia type 7 - Acute myeloblastic leukemia with maturation - Acute myeloblastic leukemia without maturation - Acute myelocytic leukemia - Acute myelogenous leukemia - Acute myeloid leukemia (generic term) - Acute myeloid leukemia, secondary - Acute myelomonocytic leukemia - Acute necrotizing ulcerative gingivitis - Acute non lymphoblastic leukemia (generic term) - Acute pancreatitis - Acute posterior multifocal placoid pigment epitheliopathy - Acute promyelocytic leukemia -

Acute r-Acute t

Acute renal failure - Acute respiratory distress syndrome - Acute tubular necrosis -

Acy

Acyl-CoA dehydrogenase, medium chain, deficiency of - Acyl-CoA dehydrogenase, short chain, deficiency of - Acyl-CoA dehydrogenase, very long chain, deficiency of - Acyl-CoA oxidase deficiency -

Ad

Ada-Adi

Adactylia unilateral dominant - Adam complex familial - Adams Nance syndrome - Adams-Oliver syndrome - Addison's disease - Adducted thumb club foot syndrome - Adducted thumb syndrome recessive form - Adducted thumbs Dundar type - Adenine phosphoribosyltransferase deficiency - Adenocarcinoid tumor - Adenocarcinoma of lung - Adenocarcinoma of Esophagus - Adenoid cystic carcinoma - Adenoma of the adrenal gland - Adenoma - Adenomelablastoma - Adenomyosis - Adenosine deaminase deficiency - Adenosine monophosphate deaminase deficiency - Adenosine triphosphatase deficiency, anemia due to - Adenylosuccinate lyase deficiency - Adie syndrome - Adiposis dolorosa aka Dercum's disease -

Ado-Adr

Adolescent benign focal crisis - Adrenal adenoma, familial - Adrenal cancer - Adrenal disorder - Adrenal gland hyperfunction - Adrenal gland hypofunction - Adrenal hyperplasia, congenital - Adrenal hyperplasia - Adrenal hypertension - Adrenal hypoplasia congenital, X-linked - Adrenal hypoplasia - Adrenal incidentaloma - Adrenal insufficiency - Adrenal macropolyadenomatosis - Adrenal medulla neoplasm - Adrenocortical carcinoma - Adrenogenital syndrome - Adrenoleukodystrophy, autosomal, neonatal form - Adrenoleukodystrophy, X-linked - Adrenoleukodystrophy - Adrenomyodystrophy -

Adu

Adult onset Still's disease - Adult Spinal Muscular Atrophy - Adult syndrome - Advanced sleep phase syndrome -

Ae-Ah

Afibrinogenemia - Agammaglobulinemia - Aganglionosis - Aganglionosis, total intestinal - Aging - Aggressive fibromatosis - Agnathia - Agnathia holoprosencephaly situs inversus - Agnosia, primary visual - Agoraphobia - Agyria - Agyria pachygyria polymicrogyria - Agyria-pachygyria type 1 - Ahumada-Del Castillo syndrome -

Ai-Ak

Aicardi syndrome - Aicardi-Goutières syndrome - Aichmophobia - AIDS - AIDS Dementia Complex - AIDS dysmorphic syndrome - Ainhum - Akaba Hayasaka syndrome - Akesson syndrome - Aksu Stckhausen syndrome -

Al

Al Awadi Teebi Farag syndrome - Al Frayh Facharzt Haque syndrome - Al Gazali Al Talabani syndrome - Al Gazali Aziz Salem syndrome - Al Gazali Donnai Mueller syndrome - Al Gazali Hirschsprung syndrome - Al Gazali Khidr Prem Chandran syndrome - Al Gazali Sabrinathan Nair syndrome -

Ala-Alc

Alagille-Watson syndrome (AWS) - Alar nasal cartilages coloboma of telecanthus - Albers-Schonberg disease - Albinism deafness syndrome - Albinism immunodeficiency - Albinism ocular late onset sensorineural deafness - Albinism oculocutaneous, Hermansky-Pudlak type - Albinism, minimal pigment type - Albinism, ocular - Albinism, yellow mutant type - Albinism - Albinoidism - Albrecht Schneider Belmont syndrome - Albright Turner Morgani syndrome - Albright's hereditary osteodystrophy - Albright's syndrome - Alcaptonuria - Alcohol antenatal infection - Alcohol fetopathy - Alcoholic hepatitis - Alcoholic liver cirrhosis -

Ald-All

Aldolase A deficiency - Aldred syndrome - Aleukemic leukemia cutis - Alexander disease - Alien hand syndrome - Alkaptonuria - Allain Babin Demarquez syndrome - Allan Herndon syndrome - Allanson Pantzar McLeod syndrome - Allergic angiitis - Allergic autoimmune thyroiditis - Allergic bronchopulmonary aspergillosis - Allergic encephalomyelitis -

Alo

Aloi Tomasini Isaia syndrome - Alopecia - Alopecia anosmia deafness hypogonadism syndrome - Alopecia areata - Alopecia congenita keratosis palmoplantaris - Alopecia contractures dwarfism mental retardation - Alopecia epilepsy oligophrenia syndrome of Moynahan - Alopecia hypogonadism extrapyramidal disorder - Alopecia immunodeficiency - Alopecia macular degeneration growth retardation - Alopecia mental retardation hypogonadism - Alopecia mental retardation syndrome - Alopecia totalis - Alopecia universalis onychodystrophy vitiligo - Alopecia universalis - Alopecia, epilepsy, pyorrhea, mental subnormality -

Alp-Alz

Alpers disease - Alpha 1-antitrypsin deficiency - Alpha-2 deficient collagen disease - Alpha-ketoglutarate dehydrogenase deficiency - Alpha-L-iduronidase deficiency - Alpha-mannosidosis - Alpha-sarcoglycanopathy - Alpha-thalassemia - Alpha-thalassemia-abnormal morphogenesis - Alport syndrome macrothrombocytopenia - Alport syndrome, dominant type - Alport syndrome, recessive type - Alport syndrome - Alstrom's syndrome - Alternating hemiplegia of childhood - Alternating hemiplegia - Aluminium lung - Alveolar Capillary Dysplasia - Alveolar echinococcosis - Alveolar soft part sarcoma - Alveolitis, extrinsic allergic - Alves Dos Santos Castello syndrome - Alzheimer's disease - Alzheimer disease, familial -

Am

Ama-Amy

Amaurosis - Amaurosis congenita of Leber, type 1 - Amaurosis congenita of Leber, type 2 - Amaurosis congenita of Leber - Amaurosis hypertrichosis - Amblyopia - Ambral syndrome - Ambras syndrome - Amegakaryocytic thrombocytopenia - Amelia (birth defect) - Amelia cleft lip palate hydrocephalus iris coloboma - Amelia facial dysmorphism - Amelia X linked - Amelogenesis - Amelogenesis Imperfecta hypomaturation type - Amelogenesis imperfecta local hypoplastic form - Amelogenesis imperfecta nephrocalcinosis - Amelogenesis imperfecta - Ameloonychohypohidrotic syndrome - Amenorrhea - American trypanosomiasis - Amyotrophic lateral sclerosis -

An

Ana-Ane

Anaphylaxis - Anaplastic thyroid cancer - Andersen's disease - Andre syndrome - Androgen insensitivity syndrome (AIS) - Anemia sideroblastic spinocerebellar ataxia - Anemia, Diamond-Blackfan - Anemia, Hypoplastic, Congenital - Anemia, Pernicious - Anemia, Sideroblastic - Anemia - Anencephaly spina bifida X linked - Anencephaly - Aneurysm of sinus of Valsalva - Aneurysm, intracranial berry - Aneurysm -

Ang

Angel shaped phalangoep - Angiofollicular lymph hyperplasia - Angioimmunoblastic lymphadenopathy with dysproteinemia - Angiokeratoma mental retardation coarse face - Angiolipoma - Angioma - Angioma hereditary neurocutaneous - Angiomatosis - Angiomatosis encephalotrigeminal - Angiomatosis leptomeningeal capillary - venous - Angiomatosis systemic cystic seip syndrome - Angiomyomatous hamartoma - Angioneurotic edema hereditary due to C1 esterase deficiency - Angiosarcoma - Angiosarcoma of the liver - Angiosarcoma of the scalp - Angiostrongyliasis - Angiotensin renin aldosterone hypertension - Anguillulosis -

Ani-Ank

Aniridia absent patella - Aniridia ataxia renal agenesis psychomotor retardation - Aniridia cerebellar ataxia mental deficiency - Aniridia mental retardation syndrome - Aniridia ptosis mental retardation obesity familial - Aniridia renal agenesis psychomotor retardation - Aniridia type 2 - Aniridia, sporadic - Aniridia - Anisakiasis - Ankle defects short stature - Ankyloblepharon ectodermal defects cleft lip palate - Ankyloblepharon filiforme adnatum cleft palate - Ankyloblepharon filiforme imperforate anus - Ankyloglossia heterochromia clasped thumbs - Ankylosing spondylarthritis - Ankylosing spondylitis - Ankylosing vertebral hyperostosis with tylosis - Ankylosis - Ankylosis of teeth - Ankylostomiasis -

Ann

Annular constricting bands - Annular pancreas - Annuloaortic ectasia -

Ano

Anodontia - Anonychia - Anonychia ectrodactyly - Anonychia microcephaly - Anonychia onychodystrophy brachydactyly type B - Anonychia onychodystrophy - Anophthalia - Anophthalia pulmonary hypoplasia - Anophthalmia - Anophthalmia cleft lip palate hypothalamic disorder - Anophthalmia cleft palate micrognathia - Anophthalmia esophageal atresia cryptorchidism - Anophthalmia megalocornea cardiopathy skeletal anomalies - Anophthalmia microcephaly hypogonadism - Anophthalmia plus syndrome - Anophthalmia short stature obesity - Anophthalmia Waardenburg syndrome - Anophthalmos - Anophthalmos with limb anomalies - Anophthalmos, clinical - Anorchia - Anorchidism - Anorectal anomalies - Anorectal atresia / Ano-rectal atresia - Anorexia nervosa - Anosmia - Anotia facial palsy cardiac defect - Anotia -

Ans-Ant

Ansell Bywaters Elderking syndrome - Anterior horn disease - Anterior pituitary insufficiency, familial - Anthrax - Anti-factor VIII autoimmunization - Antigen-peptide-transporter 2 deficiency - Anti-HLA hyperimmunization - Antihypertensive drugs antenatal infection - Antinolo Nieto Borrego syndrome - Antiphospholipid syndrome - Anti-plasmin deficiency - Anti-plasmin deficiency, congenital - Antisocial personality disorder - Antisynthetase syndrome - Antithrombin deficiency, congenital - Antley-Bixler syndrome - Anton syndrome -

Ao

Aorta-pulmonary artery fistula - Aortic aneurysm - Aortic arch anomaly peculiar facies mental retardation - Aortic arch interruption - Aortic arches defect - Aortic coarctation - Aortic dissection - Aortic dissection lentiginosis - Aortic supravalvular stenosis - Aortic valve stenosis - Aortic valves stenosis of the child - Aortic window -

Ap

Ape-App

Apert like polydactyly syndrome - Apert syndrome - Aphalangia - Aphalangia hemivertebrae - Aphalangia syndactyly microcephaly - Aphthous stomatitis - Apiphobia - Aplasia - Aplasia cutis autosomal recessive - Aplasia cutis congenita dominant - Aplasia cutis congenita epibulbar dermoids - Aplasia cutis congenita intestinal lymphangiectasia - Aplasia cutis congenita of limbs recessive - Aplasia cutis congenita recessive - Aplasia cutis congenita - Aplasia cutis myopia - Aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits and nails - Aplastic anemia - Aplastic crisis - Apo A-I deficiency - Apolipoprotein C-II deficiency - Apparent mineralocorticoid excess - Appelt-Gerken-Lenz syndrome - Appendicitis -

Apr-Apu

Apraxia manual - Apraxia, Ideomotor - Apraxia, ocular motor, Cogan type - Apraxia - Apudoma -

Aq

Aqueductal stenosis - Aqueductal stenosis, X linked -

Ar

Ara-Aro

Arachindonic acid, absence of - Arachnodactyly - Arachnodactyly ataxia cataract aminoaciduria mental retardation - Arachnodactyly mental retardation dysmorphism - Arachnoid cysts - Arachnoiditis - Arakawa's syndrome II - Arbovirosis - Arc syndrome - Aredyld syndrome - AREDYLD - Arginase deficiency - Arginemia - Argininosuccinate synthetase deficiency - Argininosuccinic aciduria - Argyria - Arhinia - Arhinia choanal atresia microphthalmia - Arnold Stickler Bourne syndrome - Arnold-Chiari malformation - Aromatase deficiency - Aromatic amino acid decarboxylase deficiency -

Arr

Arrhinia - Arrhythmogenic right ventricular dysplasia - Arroyo Garcia Cimadevilla syndrome - Arrythmogenic right ventricular dysplasia, familial -

Art

Arte

Arterial calcification of infancy - Arterial dysplasia - Arterial tortuosity - Arteriovenous malformation - Arteritis -

Arth

Arthritis short stature deafness - Arthritis, Juvenile - Arthritis - Arthrogryposis due to muscular dystrophy - Arthrogryposis ectodermal dysplasia other anomalies - Arthrogryposis epileptic seizures migrational brain disorder - Arthrogryposis IUGR thoracic dystrophy - Arthrogryposis like disorder - Arthrogryposis like hand anomaly sensorineural - Arthrogryposis multiplex congenita CNS calcification - Arthrogryposis multiplex congenita distal - Arthrogryposis multiplex congenita neurogenic type - Arthrogryposis multiplex congenita pulmonary hypoplasia - Arthrogryposis multiplex congenita whistling face - Arthrogryposis multiplex congenita, distal type 1 - Arthrogryposis multiplex congenita, distal type 2 - Arthrogryposis multiplex congenita, distal, x-linked - Arthrogryposis multiplex congenita - Arthrogryposis ophthalmoplegia retinopathy - Arthrogryposis renal dysfunction cholestasis syndrome - Arthrogryposis spinal muscular atrophy - Arthrogryposis -

Ary

Arylsulfatase A deficiency -

As

Asbestosis - Ascariasis - Ascher's syndrome - Aseptic meningitis - Asherman's syndrome - Ashman phenomenon - Aspartylglycosaminuria - Aspergillosis - Asperger syndrome - Asphyxia neonatorum - Aspiration pneumonia - Asplenia - Astasis - Astasia-abasia - Asthenia - Asthma - Astrocytoma - Asymmetric septal hypertrophy -

At

Ataxia - Ataxia telangiectasia variant V1 - Ataxia telangiectasia - Ataxia, Marie's - Atelectasis - Atelosteogenesis, type II - Athabaskan brain stem dysgenesis - Atherosclerosis - Athetosis - Athlete's foot - Atopic Dermatitis - Atresia - Atresia of small intestine - Atrial myxoma - Atrial septal defect - Atrioventricular fistula - Atrioventricular septal defect - Atrophic vaginitis - Atrophoderma - Atrophoderma of Pierini and Pasini - Atrophy - ATR-X - Attention Deficit Hyperactivity Disorder - Attenuated FAP - Atypical lipodystrophy -

Au-Az

Aughton syndrome - Ausems Wittebol Post Hennekam syndrome - Autism - Autoimmune hemolytic anemia - Autoimmune hepatitis - Autoimmune peripheral neuropathy - Autoimmune polyendocrinopathy syndrome, type I - Autonomic dysfunction - Autonomic nervous system diseases - Axial mesodermal dysplasia - Axial mesodermal dysplasia spectrum - Axial osteomalacia - Axial osteosclerosis - Ayazi syndrome -

Ba

Bab-Bam

Baber's syndrome - Babesiosis - Bacterial endocarditis - Bacterial food poisoning - Bacterial gastroenteritis - Bacterial meningitis - Bacterial pneumonia - Bacterial vaginalis - BAER - Bagatelle Cassidy syndrome - Bahemuka Brown syndrome - Baker Vinters syndrome - Baker-Winegard syndrome - Balantidiasis - Ballard syndrome - Ballistophobia - Balo disease - Balo's concentric sclerosis - Bamforth syndrome -

Ban

BANF acoustic neurinoma - Bangstad syndrome - Banki syndrome - Bannayan-Zonana syndrome - Banti's syndrome - Bantu siderosis -

Bar

Baraitser Brett Piesowicz syndrome - Baraitser Rodeck Garner syndrome - Barber Say syndrome - Bardet-Biedl syndrome, type 1 - Bardet-Biedl syndrome, type 2 - Bardet-Biedl syndrome, type 3 - Bardet-Biedl syndrome, type 4 - Bare lymphocyte syndrome 2 - Bare lymphocyte syndrome - Baritosis - Barnicoat Baraitser syndrome - Barrett syndrome - Barrow Fitzsimmons syndrome - Barth syndrome - Bartonella infections - Bartsocas Papa syndrome - Bartter syndrome, antenatal form - Bartter syndrome, classic form -

Bas-Baz

Basal cell carcinoma - Basal cell nevus anodontia abnormal bone mineralization - Basal ganglia diseases - Basan syndrome - Basaran Yilmaz syndrome - Basedow's coma - Basilar artery migraines - Basilar impression primary - Bassoe syndrome - Bathophobia - Batrachophobia - Battaglia Neri syndrome - Batten disease - Batten Turner muscular dystrophy - Baughman syndrome - Bazex-Dupre-Christol syndrome - Bazopoulou Kyrkanidou syndrome -

Bc-Bd

B-cell lymphomas - Bd syndrome -

Be

Bea-Bel

Beals syndrome - Beardwell syndrome - Bébé Collodion syndrome - Becker disease - Becker's muscular dystrophy - Becker's nevus - Beemer Ertbruggen syndrome - Beemer Langer syndrome - Behcet syndrome - Behr syndrome - Behrens Baumann Dust syndrome - Bejel - Bellini Chiumello Rinoldi syndrome - Bell's palsy -

Ben-Ber

Ben Ari Shuper Mimouni syndrome - Benallegue Lacete syndrome - Bencze syndrome - Benign astrocytoma - Benign autosomal dominant myopathy - Benign congenital hypotonia - Benign essential blepharospasm - Benign essential tremor syndrome - Benign familial hematuria - Benign familial infantile convulsions - Benign familial infantile epilepsy - Benign fasciculation syndrome - Benign lymphoma - Benign mucosal pemphigoid - Benign paroxysmal positional vertigo - Bentham Driessen Hanveld syndrome - Berardinelli-Seip congenital lipodystrophy - Berdon syndrome - Berger disease - Beriberi - Berlin Breakage syndrome - Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification - Berylliosis - Beta ketothiolase deficiency - Beta-galactosidase-1 deficiency - Beta-mannosidosis - Beta-sarcoglycanopathy - Beta-thalassemia major anemia - Beta-thalassemia (gene promoter involvement) - Bethlem myopathy -

Bh

Bhaskar Jagannathan syndrome -

Bi

Bib-Bil

Bickel Fanconi glycogenosis - Bicuspid aortic valve - Bidirectional tachycardia - Biemond syndrome type 1 - Biemond syndrome type 2 - Biemond syndrome - Biermer disease - Bifid nose dominant - Bilateral renal agenesis dominant type - Bilateral renal agenesis - Biliary atresia, extrahepatic - Biliary atresia, intrahepatic, non syndromic form - Biliary atresia, intrahepatic, syndromic form - Biliary atresia - Biliary cirrhosis - Biliary hypoplasia - Biliary malformation renal tubular insufficiency - Biliary tract cancer - Billard Toutain Maheut syndrome - Billet Bear syndrome -

Bin-Bix

Bindewald Ulmer Muller syndrome - Binswanger's disease - Bipolar disorder - Biotinidase deficiency - Bird headed dwarfism Montreal type - Birdshot chorioretinopathy - Birt-Hogg-Dube syndrome - Bixler Christian Gorlin syndrome -

Bj

Bjornstad syndrome -

Bl

Bla-Ble

Bladder neoplasm - Blaichman syndrome - Blastoma - Blastomycosis - Blepharitis - Blepharo cheilo dontic syndrome - Blepharo facio skeletal syndrome - Blepharo naso facial syndrome Van maldergem type - Blepharonasofacial malformation syndrome - Blepharophimosis nasal groove growth retardation - Blepharophimosis ptosis esotropia syndactyly short - Blepharophimosis ptosis syndactyly mental retardation - Blepharophimosis syndrome Ohdo type - Blepharophimosis, ptosis, epicanthus inversus - Blepharophimosis - Blepharoptosis aortic anomaly - Blepharoptosis cleft palate ectrodactyly dental anomalies - Blepharoptosis myopia ectopia lentis - Blepharospasm - Blethen Wenick Hawkins syndrome -

Blo-Blu

Blomstrand syndrome - Blood Coagulation Disorders, Inherited - Blood platelet disorders - Blood vessel disorder - Bloom syndrome - Blount's disease - Blue cone monochromatism - Blue diaper syndrome - Blue rubber bleb nevus -

Bo

Bod-Boo

BOD syndrome - Boder syndrome - Body dysmorphic disorder - Boil - Bone development disorder - Bone dysplasia Azouz type - Bone dysplasia corpus callosum agenesis - Bone dysplasia lethal Holmgren type - Bone dysplasia Moore type - Bone fragility craniosynostosis proptosis hydrocephalus - Bone marrow failure neurologic abnormalities - Bone marrow failure - Bone neoplasms - Bone tumor (generic term) - Bonneau-Beaumont syndrome - Bonneman Meinecke Reich syndrome - Bonnemann Meinecke syndrome - Bonnevie Ullrich Turner syndrome - Book syndrome - Boomerang dysplasia - Booth Haworth Dilling syndrome -

Bor-Boy

BOR syndrome - Borjeson Syndrome - Bork Stender Schmidt syndrome - Borreliosis - Borrone Di Rocco Crovato syndrome - Boscherini Galasso Manca Bitti syndrome - Bosma Henkin Christiansen syndrome - Bothriocephalosis - Botulism - Boucher Neuhauser syndrome - Boudhina Yedes Khiari syndrome - Bourneville's disease or Bourneville-Pringle disease - Bowen syndrome - Bowen-Conradi syndrome - Bowenoid papulosis - Bowen's disease - Bowing congenital short bones - Bowing of long bones congenital - Boylan Dew Greco syndrome -

Br

Bra

Brac

Brach

Brachi-Brachm

Brachioskeletogenital syndrome - Brachman-de Lange syndrome -

Brachy

Brachyc

Brachycephalofrontonasal dysplasia - Brachycephaly deafness cataract mental retardation -

Brachyd

Brachydactylous dwarfism Mseleni type -

Brachydactyly

Brachydactyly -

Brachydactyly a-Brachydactyly s

Brachydactyly absence of distal phalanges - Brachydactyly anonychia - Brachydactyly clinodactyly - Brachydactyly dwarfism mental retardation - Brachydactyly elbow wrist dysplasia - Brachydactyly hypertension - Brachydactyly long thumb type - Brachydactyly mesomelia mental retardation heart defects - Brachydactyly nystagmus cerebellar ataxia - Brachydactyly preaxial hallux varus - Brachydactyly scoliosis carpal fusion - Brachydactyly small stature face anomalies - Brachydactyly Smorgasbord type -

Brachydactyly t

Brachydactyly tibial hypoplasia - Brachydactyly type A1 - Brachydactyly type A2 - Brachydactyly type A3 - Brachydactyly type A5 nail dysplasia - Brachydactyly type A6 - Brachydactyly type A7 - Brachydactyly type B - Brachydactyly type C - Brachydactyly type E - Brachydactyly types B and E combined -

Brachym-Brachyt

Brachymesomelia renal syndrome - Brachymesophalangy 2 and 5 - Brachymesophalangy mesomelic short limbs osseous anomalies - Brachymesophalangy type 2 - Brachymetapody anodontia hypotrichosis albinoidism - Brachymorphism onychodysplasia dysphalangism syndrome - Brachyolmia recessive Hobaek type - Brachyolmia - Brachytelephalangy characteristic facies Kallmann -

Brad-Bran

Braddock Carey syndrome - Braddock Jones Superneau syndrome - Bradykinesia - Brain cavernous angioma - Brain Neoplasms - Brain Stem Neoplasms - Branchial arch defects - Branchial arch syndrome X linked - Branchio oculo facial syndrome Hing type - Branchio-oculo-facial syndrome - Branchiootorenal syndrome -

Bre-Bro

Breast and ovarian cancer - Breast cancer, familial - Bright's disease - Brittle bone disease - Brittle bone syndrome lethal type - Brittle cornea syndrome - Broad beta disease - Broad-betalipoproteinemia - Bromidrosiphobia - Bronchiectasis - Bronchiectasis oligospermia - Bronchiolitis obliterans with obstructive pulmonary disease - Bronchiolotis obliterans organizing pneumonia (BOOP) - Bronchitis, Chronic - Bronchogenic cyst - Bronchopulmonary amyloidosis - Bronchopulmonary dysplasia - Brown syndrome - Brown-Séquard syndrome -

Bru

Brucellosis - Bruck syndrome - Brugada syndrome - Brunoni syndrome - Bruton type agammaglobulinemia - Bruyn Scheltens syndrome -

Bu-Bz

Bubonic plague - Budd-Chiari syndrome - Buerger's disease - Bulbospinal amyotrophy, X-linked - Bulimia nervosa - Bull Nixon syndrome - Bullous dystrophy macular type - Bullous ichtyosiform erythroderma congenita - Bullous pemphigoid - Buntinx Lormans Martin syndrome - Burkitt's lymphoma - Burn Goodship syndrome - Burnett Schwartz Berberian syndrome - Burning mouth syndrome- Type 3 - Burning mouth syndrome - Buschke Ollendorff syndrome - Bustos Simosa Pinto Cisternas syndrome - Buttiens Fryns syndrome - Butyrylcholinesterase deficiency - Byssinosis -

C

C syndrome - C1 esterase deficiency (angioedema) -

Ca

Cac-Cal

Cacchi-Ricci disease - CACH syndrome - Cafe au lait spots syndrome - Caffey disease - CAHMR syndrome - Calcinosis cutis (see also CREST syndrome) - Calciphylaxis - Calculi - Calderon Gonzalez Cantu syndrome - Calloso genital dysplasia - Callus disease - Calpainopathy - Calvarial hyperostosis -

Cam-Can

Camera Marugo -Cohen syndrome - Camfak syndrome - Campomelia Cumming type - Camptobrachydactyly - Camptocormism - Camptodactyly fibrous tissue hyperplasia skeletal dysplasia - Camptodactyly joint contractures facial skeletal dysplasia - Camptodactyly overgrowth unusual facies - Camptodactyly syndrome Guadalajara type 1 - Camptodactyly syndrome Guadalajara type 2 - Camptodactyly taurinuria - Camptodactyly vertebral fusion - Camptomelic syndrome - Campylobacter infection - Camurati Engelmann disease - Canavan leukodystrophy - Cancer - Candidiasis familial chronic - Candidiasis - Canga's bead symptom - Canine distemper - Cantalamessa Baldini Ambrosi syndrome - Cantu Sanchez Corona Fragoso syndrome - Cantu Sanchez Corona Garcia syndrome - Cantu Sanchez Corona Hernandes syndrome -

Cap

Capillary leak syndrome with monoclonal gammopathy - Capillary venous leptomeningeal angiomatosis - Caplan's syndrome - Capos syndrome -

Car

Cara-Carc

Caratolo Cilio Pessagno syndrome - Carbamoyl phosphate synthetase deficiency - Carbamoyl-phosphate synthase I deficiency disease (ornithine carbamoyl phosphate deficiency) - Carbohydrate deficient glycoprotein syndrome - Carbon baby syndrome - Carbonic anhydrase II deficiency - Carcinoid syndrome - Carcinoma of the vocal tract - Carcinoma, squamous cell of head and neck - Carcinoma, squamous cell - Carcinophobia -

Card

Cardi

Cardia

Cardiac amyloidosis - Cardiac and laterality defects - Cardiac arrest - Cardiac conduction defect, familial - Cardiac diverticulum - Cardiac hydatid cysts with intracavitary expansion - Cardiac malformation - Cardiac tamponade - Cardiac valvular dysplasia, X-linked - pernambuco viadim -

Cardio

Cardioauditory syndrome of Sanchez- Cascos - Cardioauditory syndrome - Cardiofacial syndrome short limbs - Cardiofaciocutaneous syndrome - Cardiogenital syndrome - Cardiomelic syndrome Stratton Koehler type - Cardiomyopathy:
Arrhythmogenic right ventricular cardiomyopathy - Cardiomyopathic lentiginosis - Cardiomyopathy cataract hip spine disease - Cardiomyopathy diabetes deafness - Dilated cardiomyopathy: Cardiomyopathy dilated with conduction defect type 1, Cardiomyopathy dilated with conduction defect type 2, Cardiomyopathy, familial dilated - Cardiomyopathy due to anthracyclines - Cardiomyopathy hearing loss type t RNA lysine gene mutation - Hypertrophic cardiomyopathy: familial - Cardiomyopathy hypogonadism metabolic anomalies - Cardiomyopathy spherocytosis - Cardiomyopathy, fatal fetal, due to myocardial calcification - Cardiomyopathy, X linked, fatal infantile - Restrictive cardiomyopathy -
- Cardioskeletal myopathy-neutropenia - Cardiospasm -

Care-Carr

Carey Fineman Ziter syndrome - Carnevale Canun Mendoza syndrome - Carnevale Hernandez Castillo syndrome - Carnevale Krajewska Fischetto syndrome - Carney syndrome - Carnitine palmitoyl transferase 1 deficiency - Carnitine palmitoyl transferase 2 deficiency - Carnitine palmitoyl transferase deficiency - Carnitine transporter deficiency - Carnitine-acylcarnitine translocase deficiency - Carnosinase deficiency - Carnosinemia - Caroli disease - Carotenemia - Carotid artery dissection - Carpal deformity migrognathia microstomia - Carpal tunnel syndrome - Carpenter Hunter type - Carpenter syndrome - Carpo tarsal osteolysis recessive - Carpotarsal osteochondromatosis - Carrington syndrome -

Cart

Cartilage-hair hypoplasia - Cartilage hair hypoplasia like syndrome - Cartilaginous neoplasms - Cartwright Nelson Fryns syndrome -

Cas

Cassia Stocco Dos Santos syndrome - Castleman's disease - Castro Gago Pombo Novo syndrome -

Cat

Cat cry syndrome - see Cri du chat - Cat Eye syndrome - Cat Rodrigues syndrome - Cat-scratch disease -

Cata

Cataract,congenital ichthyosis - Cataract aberrant oral frenula growth retardation - Cataract anterior polar dominant - Cataract ataxia deafness - Cataract cardiomyopathy - Cataract congenital autosomal dominant - Cataract congenital dominant non nuclear - Cataract congenital Volkmann type - Cataract congenital with microphthalmia - Cataract dental syndrome - Cataract Hutterite type - Cataract hypertrichosis mental retardation - Cataract mental retardation hypogonadism - Cataract microcornea syndrome - Cataract microphthalmia septal defect - Cataract skeletal anomalies - Cataract, alopecia, sclerodactyly - Cataract, congenital, with microcornea or slight microphthalmia - Cataract, total congenital - Cataract-glaucoma -

Catc-Cate

CATCH 22 syndrome - Catecholamine hypertension - Catel Manzke syndrome -

Cau-Cay

Caudal appendage deafness - Caudal duplication - Caudal regression syndrome - Causalgia - Cavernous hemangioma - Cavernous lymphangioma - Cavernous sinus thrombosisdicks get smaller -

Cayler syndrome -

Cc-Cd

CCA syndrome - Ccge syndrome - CCHS - CDG syndrome type 1A - CDG syndrome type 1B - CDG syndrome type 1C - CDG syndrome type 2 - CDG syndrome type 3 - CDG syndrome type 4 - CDG syndrome - CDK4 linked melanoma -

Ce

Cec-Cep

Cecato De lima Pinheiro syndrome - Celiac disease epilepsy occipital calcifications - Celiac sprue - Cenani Lenz syndactylism - Cennamo Gangemi syndrome - Central core disease - Central diabetes insipidus - Central nervous system protozoal infections - Central serous chorioretinopathy - Central type neurofibromatosis - Centromeric instability immunodeficiency syndrome - Centronuclear myopathy - Centrotemporal epilepsy - Cephalopolysyndactyly -

Cer

Cera

Ceramidase deficiency - Ceramide trihexosidosis - Ceraunophobia -

Cere

Cereb

Cerebe

Cerebellar agenesis - Cerebellar ataxia areflexia pes cavus optic atrophy - Cerebellar ataxia ectodermal dysplasia - Cerebellar ataxia infantile with progressive external ophthalmoplegia - Cerebellar ataxia, dominant pure - Cerebellar degeneration, subacute - Cerebellar degeneration - Cerebellar hypoplasia endosteal sclerosis - Cerebellar hypoplasia tapetoretinal degeneration - Cerebellar hypoplasia - Cerebellar parenchymal degeneration - Cerebelloolivary atrophy - Cerebelloparenchymal disorder 3 - Cerebellum agenesis hydrocephaly -

Cerebr

Cerebral amyloid angiopathy, familial - Cerebral amyloid angiopathy - Cerebral aneurysm - Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy - Cerebral calcification cerebellar hypoplasia - Cerebral calcifications opalescent teeth phosphaturia - Cerebral cavernous malformation - Cerebral cavernous malformations - Cerebral gigantism jaw cysts - Cerebral gigantism - Cerebral hypoxia - Cerebral malformations hypertrichosis claw hands - Cerebral palsy - Cerebral thrombosis - - Cerebral ventricle neoplasm - Cerebro facio articular syndrome - Cerebro facio thoracic dysplasia - Cerebro oculo dento auriculo skeletal syndrome - Cerebro oculo genital syndrome - Cerebro oculo skeleto renal syndrome - Cerebro reno digital syndrome - Cerebroarthrodigital syndrome - Cerebro-costo-mandibular syndrome - Cerebro-oculo-facio-skeletal syndrome - Cerebroretinal vasculopathy -

Cero-Cerv

Ceroid lipofuscinois, neuronal 1, infantile - Ceroid lipofuscinois, neuronal 2, late infantile - Ceroid lipofuscinois, neuronal 3, juvenile - Ceroid lipofuscinois, neuronal 4, adult type - Ceroid lipofuscinois, neuronal 5, late infantile - Ceroid lipofuscinois, neuronal 6, late infantile - Ceroid lipofuscinois, neuronal - Ceroid lipofuscinosis, neuronal 4 - Cervical cancer - Cervical hypertrichosis neuropathy - Cervical hypertrichosis peripheral neuropathy - Cervical ribs sprengel anomaly polydactyly - Cervical vertebral fusion - Cervicooculoacoustic syndrome -

Ch

Cha

Chag-Chao

Chagas disease - Chalazion - Chanarin disease - Chanarin Dorfman syndrome ichthyosis - Chancroid - Chandler's syndrome - Chands syndrome - Chang Davidson Carlson syndrome - Chaotic atrial tachycardia -

Char

Char syndrome -

Charc

Charco

Charcot Charcot d

Charcot disease -

Charcot Marie Tooth disease

Charcot Marie tooth disease deafness dominant type - Charcot Marie tooth disease deafness mental retardation - Charcot Marie Tooth disease deafness recessive type - Charcot Marie Tooth type 1 aplasia cutis congenita - Charcot-Marie-Tooth disease type 1A - Charcot-Marie-Tooth disease type 1B - Charcot-Marie-Tooth disease type 1C - Charcot-Marie-Tooth disease type 2A - Charcot-Marie-Tooth disease type 2B1 - Charcot-Marie-Tooth disease type 2B2 - Charcot-Marie-Tooth disease type 2C - Charcot-Marie-Tooth disease type 2D - Charcot-Marie-Tooth disease type 4A - Charcot-Marie-Tooth disease type 4B - Charcot-Marie-Tooth disease with ptosis and parkinsonism - Charcot-Marie-Tooth disease, intermediate form - Charcot-Marie-Tooth disease, neuronal, type A - Charcot-Marie-Tooth disease, neuronal, type B - Charcot-Marie-Tooth disease, neuronal, type D - Charcot-Marie-Tooth disease, X-linked type 2, recessive - Charcot-Marie-Tooth disease, X-linked type 3, recessive - Charcot-Marie-Tooth disease - Charcot-Marie-Tooth peroneal muscular atrophy, X-linked -

Charg-Charl

CHARGE Association - Charles' Disease - Charlie M syndrome -

Chav

Chavany-Brunhes syndrome -

Che

Chediak-Higashi syndrome - Cheilitis glandularis - Chemke Oliver Mallek syndrome - Chemodectoma - Chemophobia - Chen Kung Ho Kaufman Mcalister syndrome - Cherubism -

Chi-Chl

Chiari type 1 malformation - Chiari-Frommel syndrome - Chickenpox - Chikungunya - CHILD syndrome ichthyosis - Childhood disintegrative disorder - Childhood pustular psoriasis - Chimerism - Chinese restaurant syndrome - Chitayat Haj Chahine syndrome - Chitayat Meunier Hodgkinson syndrome - Chitayat Moore Del Bigio syndrome - Chitty Hall Baraitser syndrome - Chitty Hall Webb syndrome - Chlamydia trachomatis - Chlamydia - Chlamydia pneumoniae - Chlamydial and Gonococcal Conjunctivitis -

Cho

Choa-Chol

Choanal atresia deafness cardiac defects dysmorphia - Cholangiocarcinoma - Cholangitis, primary sclerosing - Cholecystitis - Choledochal cyst, hand malformation - Cholelithiasis - Cholemia, familial - Cholera - Cholestasis pigmentary retinopathy cleft palate - Cholestasis, progressive familial intrahepatic 1 - Cholestasis, progressive familial intrahepatic 2 - Cholestasis, progressive familial intrahepatic 3 - Cholestasis, progressive familial intrahepatic - Cholestasis - Cholestatic jaundice renal tubular insufficiency - Cholesterol ester storage disease - Cholesterol esterification disorder - Cholesterol pneumonia -

Chon

Chondroblastoma - Chondrocalcinosis familial articular - Chondrocalcinosis - Chondrodysplasia lethal recessive - Chondrodysplasia pseudohermaphrodism syndrome - Chondrodysplasia punctata 1, x-linked recessive - Chondrodysplasia punctata with steroid sulfatase deficiency - Chondrodysplasia punctata, brachytelephalangic - Chondrodysplasia punctata, Sheffield type - Chondrodysplasia punctata - Chondrodysplasia situs inversus imperforate anus polydactyly - Chondrodysplasia, Grebe type - Chondrodystrophy - Chondroectodermal dysplasia - Chondroma (benign) - Chondromalacia - Chondromatosis (benign) - Chondrosarcoma (malignant) - Chondrysplasia punctata, humero-metacarpal type -

Chor

Chordoma - Chorea acanthocytosis - Chorea familial benign - Chorea minor - Chorea - Choreoacanthocytosis amyotrophic - Choreoathetosis familial paroxysmal - Choriocarcinoma - Chorioretinitis - Chorioretinopathy dominant form microcephaly - Choroid plexus cyst - Choroid plexus neoplasms - Choroidal atrophy alopecia - Choroideremia hypopituitarism - Choroideremia - Choroiditis, serpiginous - Choroiditis - Choroido cerebral calcification syndrome infantile -

Chr

Chri

Christian Demyer Franken syndrome - Christian Johnson Angenieta syndrome - Christian syndrome - Christianson Fourie syndrome - Christmas disease -

Chro

Chrom

Chromhidrosis -

Chromo

Chromom-Chromop

Chromomycosis - Chromophobe renal carcinoma -

Chromos Chromosoma

Chromosomal triplication -

Chromosome Chromosome 1

Chromosome 1 ring - Chromosome 1, 1p36 deletion syndrome - Chromosome 1, deletion q21 q25 - Chromosome 1, duplication 1p21 p32 - Chromosome 1, monosomy 1p - Chromosome 1, monosomy 1p22 p13 - Chromosome 1, monosomy 1p31 p22 - Chromosome 1, monosomy 1p32 - Chromosome 1, monosomy 1p34 p32 - Chromosome 1, monosomy 1q25 q32 - Chromosome 1, monosomy 1q32 q42 - Chromosome 1, monosomy 1q4 - Chromosome 1, q42 11 q42 12 duplication - Chromosome 1, trisomy 1q32 qter - Chromosome 1, trisomy 1q42 qter - Chromosome 1, uniparental disomy 1q12 q21 -

Chromosome 10-Chromosome 12

Chromosome 10 ring - Chromosome 10, distal trisomy 10q - Chromosome 10, monosomy 10p - Chromosome 10, monosomy 10q - Chromosome 10, trisomy 10p - Chromosome 10, trisomy 10pter p13 - Chromosome 10, trisomy 10q - Chromosome 10, uniparental disomy of - Chromosome 10p terminal deletion syndrome - Chromosome 11, deletion 11p - Chromosome 11, partial trisomy 11q - Chromosome 11-14 translocation - Chromosome 11p, partial deletion - Chromosome 11q partial deletion - Chromosome 11q trisomy - Chromosome 12 ring - Chromosome 12, 12p trisomy - Chromosome 12, trisomy 12q - Chromosome 12p deletion - Chromosome 12p partial deletion -

Chromosome 13-Chromosome 15

Chromosome 13 duplication - Chromosome 13 ring - Chromosome 13, partial monosomy 13q - Chromosome 13p duplication - Chromosome 13q deletion - Chromosome 13q trisomy - Chromosome 13q-mosaicism - Chromosome 14 ring - Chromosome 14 trisomy - Chromosome 14, deletion 14q, partial duplication 14p - Chromosome 14, trisomy mosaic - Chromosome 14q, partial deletions - Chromosome 14q, proximal duplication - Chromosome 14q, terminal deletion - Chromosome 14q, terminal duplication - Chromosome 15 ring - Chromosome 15, distal trisomy 15q - Chromosome 15, trisomy mosaicism - Chromosome 15q, partial deletion - Chromosome 15q, tetrasomy - Chromosome 15q, trisomy -

Chromosome 16-Chromosome 1q

Chromosome 16, trisomy 16p - Chromosome 16, trisomy 16q - Chromosome 16, trisomy - Chromosome 16, uniparental disomy - Chromosome 17 trisomy - Chromosome 17 deletion - Chromosome 17 ring - Chromosome 17, deletion 17q23 q24 - Chromosome 17, trisomy 17p - Chromosome 17, trisomy 17p11 2 - Chromosome 17, trisomy 17q22 - Chromosome 18 long arm deletion syndrome - Chromosome 18 mosaic monosomy - Chromosome 18 ring - Chromosome 18, deletion 18q23 - Chromosome 18, monosomy 18p - Chromosome 18, tetrasomy 18p - Chromosome 18, trisomy 18p - Chromosome 18, trisomy 18q - Chromosome 18, trisomy - Chromosome 19 ring - Chromosome 19, trisomy 19q - Chromosome 1q, duplication 1q12 q21 -

Chromosome 2

Chromosome 2, monosomy 2p22 - Chromosome 2, monosomy 2pter p24 - Chromosome 2, monosomy 2q - Chromosome 2, monosomy 2q24 - Chromosome 2, monosomy 2q37 - Chromosome 2, trisomy 2p - Chromosome 2, Trisomy 2p13 p21 - Chromosome 2, trisomy 2pter p24 - Chromosome 2, trisomy 2q - Chromosome 2, trisomy 2q37 -

Chromosome 20-Chromosome 22

Chromosome 20 ring - Chromosome 20, deletion 20p - Chromosome 20, duplication 20p - Chromosome 20, trisomy - Chromosome 21 monosomy - Chromosome 21 ring - Chromosome 21, monosomy 21q22 - Chromosome 21, tetrasomy 21q - Chromosome 21, uniparental disomy of - Chromosome 22 ring - Chromosome 22 trisomy mosaic - Chromosome 22, microdeletion 22 q11 - Chromosome 22, monosome mosaic - Chromosome 22, trisomy q11 q13 - Chromosome 22, trisomy -

Chromosome 3

Chromosome 3 duplication syndrome - Chromosome 3, monosomy 3p - Chromosome 3, monosomy 3p14 p11 - Chromosome 3, monosomy 3p2 - Chromosome 3, monosomy 3p25 - Chromosome 3, monosomy 3q13 - Chromosome 3, monosomy 3q21 23 - Chromosome 3, monosomy 3q27 - Chromosome 3, trisomy 3p - Chromosome 3, trisomy 3p25 - Chromosome 3, trisomy 3q - Chromosome 3, trisomy 3q13 2 q25 - Chromosome 3, Trisomy 3q2 -

Chromosome 4-Chromosome 5

Chromosome 4 ring - Chromosome 4 short arm deletion - Chromosome 4, monosomy 4p14 p16 - Chromosome 4, monosomy 4q - Chromosome 4, monosomy 4q32 - Chromosome 4, monosomy distal 4q - Chromosome 4, partial trisomy distal 4q - Chromosome 4, Trisomy 4p - Chromosome 4, trisomy 4q - Chromosome 4, trisomy 4q21 - Chromosome 4, trisomy 4q25 qter - Chromosome 5, monosomy 5q35 - Chromosome 5, trisomy 5p - Chromosome 5, trisomy 5pter p13 3 - Chromosome 5, trisomy 5q - Chromosome 5, uniparental disomy -

Chromosome 6-Chromosome 7

Chromosome 6 ring - Chromosome 6, deletion 6q13 q15 - Chromosome 6, monosomy 6p23 - Chromosome 6, monosomy 6q - Chromosome 6, monosomy 6q1 - Chromosome 6, monosomy 6q2 - Chromosome 6, partial trisomy 6q - Chromosome 6, trisomy 6p - Chromosome 6, trisomy 6q - Chromosome 7 ring - Chromosome 7, monosomy 7q2 - Chromosome 7, monosomy 7q21 - Chromosome 7, monosomy 7q3 - Chromosome 7, monosomy - Chromosome 7, partial monosomy 7p - Chromosome 7, trisomy 7p - Chromosome 7, trisomy 7p13 p12 2 - Chromosome 7, trisomy 7q - Chromosome 7, trisomy mosaic -

Chromosome 8-Chromosome 9

Chromosome 8 deletion - Chromosome 8 ring - Chromosome 8, monosomy 8p - Chromosome 8, monosomy 8p2 - Chromosome 8, monosomy 8p23 1 - Chromosome 8, monosomy 8q - Chromosome 8, mosaic trisomy - Chromosome 8, partial trisomy - Chromosome 8, trisomy 8p - Chromosome 8, trisomy 8q - Chromosome 8, trisomy - Chromosome 9 inversion or duplication - Chromosome 9 Ring - Chromosome 9, duplication 9q21 - Chromosome 9, monosomy 9p - Chromosome 9, partial monosomy 9p - Chromosome 9, partial trisomy 9p - Chromosome 9, tetrasomy 9p - Chromosome 9, trisomy 9q - Chromosome 9, trisomy 9q32 - Chromosome 9, trisomy mosaic - Chromosome 9, trisomy -

Chromosomes

Chromosomes 1 and 2, monosomy 2q duplication 1p -

Chron

Chronic berylliosis - Chronic demyelinizing neuropathy with IgM monoclonal - Chronic erosive gastritis - Chronic fatigue immune dysfunction syndrome - Chronic fatigue syndrome - Chronic granulomatous disease - Chronic hiccup - Chronic inflammatory demyelinating polyneuropathy - Chronic lymphocytic leukemia - Chronic mountain sickness - Chronic myelogenous leukemia - Chronic myelomonocytic leukemia - Chronic necrotizing vasculitis - Chronic neutropenia - Chronic obstructive pulmonary disease - Chronic polyradiculoneuritis - Chronic recurrent multifocal osteomyelitis - Chronic renal failure - Chronic spasmodic dysphonia - Chronic, infantile, neurological, cutaneous, articular syndrome -

Chu-Chy

Chudley Lowry Hoar syndrome - Chudley Rozdilsky syndrome - Chudley-Mccullough syndrome - Churg-Strauss syndrome - Chylous ascites -

Ci

Cicatricial pemphigoid - Ciguatera fish poisoning - Ciliary discoordination, due to random ciliary orientation - Ciliary dyskinesia, due to transposition of ciliary microtubules - Ciliary dyskinesia-bronchiectasis - Cilliers Beighton syndrome - Cinchonism - Circumscribed cutaneous aplasia of the vertex - Circumscribed disseminated keratosis Jadassohn Lew type - Citrullinemia -

Cl

Cla

Clarkson disease - Clayton Smith Donnai syndrome -

Cle

Clef

Cleft

Cleft h-Cleft l

Cleft hand absent tibia - Cleft lip and palate malrotation cardiopathy - Cleft lip and/or palate with mucous cysts of lower - Cleft lip palate abnormal thumbs microcephaly - Cleft lip palate deafness sacral lipoma - Cleft lip palate dysmorphism Kumar type - Cleft lip palate ectrodactyly - Cleft lip palate incisor and finger anomalies - Cleft lip palate mental retardation corneal opacity - Cleft lip palate oligodontia syndactyly pili torti - Cleft lip palate pituitary deficiency - Cleft lip palate-tetraphocomelia - Cleft lip with or without cleft palate - Cleft lip - Cleft lower lip cleft lateral canthi chorioretinal -

Cleft p-Cleft u

Cleft palate cardiac defect ectrodactyly - Cleft palate colobomata radial synostosis deafness - Cleft palate heart disease polydactyly absent tibia - Cleft palate lateral synechia syndrome - Cleft palate short stature vertebral anomalies - Cleft palate stapes fixation oligodontia - Cleft palate X linked - Cleft palate - Cleft tongue syndrome - Cleft upper lip median cutaneous polyps -

Clefti

Clefting ectropion conical teeth -

Clei

Cleidocranial dysplasia micrognathia absent thumbs - Cleidocranial dysplasia -

Cli-Clu

Cloacal exstrophy - Clouston syndrome - Cloverleaf skull bone dysplasia - Cloverleaf skull micromelia thoracic dysplasia - Clubfoot - Cluster headache -

Cm

CMV antenatal infection -

Co

Coa-Cof

Coach syndrome - Coal workers' pneumoconiosis - Coarctation of aorta dominant - Coarse face hypotonia constipation - Coats disease - Coeliac disease - Cocaine antenatal infection - Cocaine fetopathy - Coccidioidomycosis - Cochin Jewish Disorder - Cockayne syndrome type 1 - Cockayne syndrome type 2 - Cockayne syndrome type 3 - Cockayne's syndrome - Codas syndrome - Coenzyme Q cytochrome c reductase deficiency of - Coffin-Lowry syndrome - Coffin-Siris syndrome - COFS syndrome -

Cog-Coh

Cogan-Reese syndrome - Cogan syndrome - Cohen Hayden syndrome - Cohen Lockood Wyborney syndrome - Cohen syndrome -

Col

Cola-Coll

Colavita Kozlowski syndrome - Cold agglutination syndrome - Cold agglutinin disease - Cold antibody hemolytic anemia - Cold contact urticaria - Cold urticaria - Cole carpenter syndrome - Coleman Randall syndrome - Colitis - Collagen disorder - Collagenous colitis - Collins Pope syndrome - Collins Sakati syndrome -

Colo-Colv

Coloboma chorioretinal cerebellar vermis aplasia - Coloboma hair abnormality - Coloboma of choroid and retina - Coloboma of eye lens - Coloboma of iris - Coloboma of lens ala nasi - Coloboma of macula type B brachydactyly - Coloboma of macula - Coloboma of optic nerve - Coloboma of optic papilla - Coloboma porencephaly hydronephrosis - Coloboma uveal with cleft lip palate and mental retardation - Coloboma, ocular - Colobomata unilobar lung heart defect - Colobomatous microphthalmia heart disease hearing - Colobomatous microphthalmia - Colon cancer, familial nonpolyposis - Colonic atresia - Colonic malakoplakia - Color blindness - Colorado tick fever - Colver Steer Godman syndrome -

Com

Combarros Calleja Leno syndrome - Combined hyperlipidemia, familial - Common cold - Common mesentery - Common variable immunodeficiency - Compartment syndrome - Complement component 2 deficiency - Complement component receptor 1 - Complete atrioventricular canal - Complex 1 mitochondrial respiratory chain deficiency - Complex 2 mitochondrial respiratory chain deficiency - Complex 3 mitochondrial respiratory chain deficiency - Complex 4 mitochondrial respiratory chain deficiency - Complex 5 mitochondrial respiratory chain deficiency - Complex regional pain syndrome -

Con

Cond-Cone

Conductive deafness malformed external ear - Conductive hearing loss - Condyloma acuminatum - Condyloma - Cone dystrophy - Cone rod dystrophy amelogenesis imperfecta - Cone rod dystrophy -

Cong

Conge

Congen

Congenital a-Congenital b

Congenital absence of the uterus and vagina - Congenital adrenal hyperplasia type 1 - Congenital adrenal hyperplasia type 2 - Congenital adrenal hyperplasia type 3 - Congenital adrenal hyperplasia type 4 - Congenital adrenal hyperplasia type 5 - Congenital adrenal hyperplasia - Congenital afibrinogenemia - Congenital alopecia X linked - Congenital amputation - Congenital aneurysms of the great vessels - Congenital antithrombin III deficiency - Congenital aplastic anemia - Congenital arteriovenous shunt - Congenital articular rigidity - Congenital benign spinal muscular atrophy dominant - Congenital brain disorder - Congenital bronchobiliary fistula -

Congenital c-Congenital g

Congenital cardiovascular disorder - Congenital cardiovascular malformations - Congenital cardiovascular shunt - Congenital constricting band - Congenital contractual arachnodactyly - Congenital contractures - Congenital craniosynostosis maternal hyperthyroiditis - Congenital cystic adenomatoid malformation - Congenital cystic eye multiple ocular and intracranial anomalies - Congenital cytomegalovirus - Congenital deafness - Congenital diaphragmatic hernia - Congenital erythropoietic porphyria - Congenital facial diplegia - Congenital fiber type disproportion - Congenital gastrointestinal disorder - Congenital generalized fibromatosis - Congenital giant megaureter -

Congenital h-Congenital l

Congenital heart block - Congenital heart disease ptosis hypodontia craniostosis - Congenital heart disease radio ulnar synostosis mental retardation - Congenital heart disorder - Congenital heart septum defect - Congenital hemidysplasia with ichtyosiform erythroderma and limbs defects - Congenital hemolytic anemia - Congenital hepatic fibrosis - Congenital hepatic porphyria - Congenital herpes simplex - Congenital hypomyelination neuropathy - Congenital hypothyroidism - Congenital hypotrichosis milia - Congenital ichthyosis, microcephalus, quadriplegia - Congenital ichthyosis - Congenital ichtyosiform erythroderma - Congenital insensitivity to pain with anhidrosis - Congenital kidney disorder - Congenital limb deficiency - Congenital lobar emphysema -

Congenital m-Congenital s

Congenital megacolon - Congenital megalo-ureter - Congenital mesoblastic nephroma - Congenital microvillous atrophy - Congenital mitral malformation - Congenital mitral stenosis - Congenital mixovirus - Congenital mumps - Congenital muscular dystrophy syringomyelia - Congenital myopathy - Congenital nephrotic syndrome - Congenital nonhemolytic jaundice - Congenital rubella - Congenital short bowel - Congenital short femur - Congenital skeletal disorder - Congenital skin disorder - Congenital spherocytic anemia - Congenital spherocytic hemolytic anemia - Congenital stenosis of cervical medullary canal - Congenital sucrose isomaltose malabsorption - Congenital syphilis -

Congenital t-Congenital v

Congenital toxoplasmosis - Congenital unilateral pulmonary hypoplasia - Congenital vagal hyperreflexivity - Congenital varicella syndrome -

Conges

Congestive heart disease -

Conju

Conjunctivitis ligneous - Conjunctivitis with Pseudomembrane - Conjunctivitis -

Conn-Conv

Connective tissue dysplasia Spellacy type - Connexin 26 anomaly - Conn's syndrome - Conotruncal heart malformations - Conradi-Hünermann syndrome - Constitutional growth delay - Constrictive bronchiolitis - Continuous muscle fiber activity hereditary - Continuous spike-wave during slow sleep syndrome - Contractural arachnodactyly - Contractures ectodermal dysplasia cleft lip palate - Contractures hyperkeratosis lethal - Contractures of feet-muscle atrophy-oculomotor apraxia - Conversion disorder - Convulsions benign familial neonatal dominant form - Convulsions benign familial neonatal -

Coo-Cop

Cooks syndrome - Cooley's anemia - Copper deficiency familial benign - Copper transport disease - Coproporhyria -

Cor

Cor biloculare - Cor pulmonale - Cor triatriatum -

Corm-Coro

Cormier Rustin Munnich syndrome - Corneal anesthesia deafness mental retardation - Corneal cerebellar syndrome - Corneal crystals myopathy neuropathy - Corneal dystrophy - Corneal endothelium dystrophy - Cornelia de Lange syndrome - Corneodermatoosseous syndrome - Coronal synostosis syndactyly jejunal atresia - Coronaro-cardiac fistula - Coronary arteries congenital malformation - Coronary artery aneurysm - Coronary heart disease -

Corp-Cort

Corpus callosum agenesis - Corpus callosum dysgenesis - Corsello Opitz syndrome - Cortada Koussef Matsumoto syndrome - Cortes Lacassie syndrome - Cortical blindness mental retardation polydactyly - Cortical degeneration of the cerebellum parenchymatous - cortical dysplasia - Cortical hyperostosis syndactyly - Corticobasal degeneration -

Cos-Cox

Costello syndrome - Costochondritis (otherwise Costal chondritis) - Costocoracoid ligament congenitally short - Cote Adamopoulos Pantelakis syndrome - Cote Katsantoni syndrome - Cousin Walbraum Cegarra syndrome - Count Choculitis - Covesdem syndrome - Cowchock Wapner Kurtz syndrome - Cowden's disease - Cowpox - Coxoauricular syndrome -

Cr

Cra

Cram

Cramer Niederdellmann syndrome - Cramp - Cramp-fasciculations syndrome -

Cran

Crand-Crane

Crandall syndrome - Crane-Heise syndrome -

Crani

Cranio

Cranio osteoarthropathy -

Cranioa-Craniom

Cranioacrofacial syndrome - Craniodiaphyseal dysplasia - Craniodigital syndrome mental retardation - Cranioectodermal dysplasia - Craniofacial and osseous defects mental retardation - Craniofacial and skeletal defects - Craniofacial deafness hand syndrome - Craniofacial dysostosis arthrogryposis progeroid appearance - Craniofacial dysostosis - Craniofacial dysynostosis - Craniofaciocardioskeletal syndrome - Craniofaciocervical osteoglyphic dysplasia - Craniofrontonasal dysplasia - Craniofrontonasal syndrome Teebi type - Craniometaphyseal dysplasia dominant type - Craniometaphyseal dysplasia recessive type - Craniomicromelic syndrome -

Cranios-Craniot

Craniostenosis cataract - Craniostenosis with congenital heart disease mental retardation - Craniostenosis - Craniosynostosis alopecia brain defect - Craniosynostosis arthrogryposis cleft palate - Craniosynostosis autosomal dominant - Craniosynostosis cleft lip palate arthrogryposis - Craniosynostosis contractures cleft - Craniosynostosis exostoses nevus epibulbar dermoid - Craniosynostosis fibular aplasia - Craniosynostosis Fontaine type - Craniosynostosis Maroteaux Fonfria type - Craniosynostosis mental retardation clefting syndrome - Craniosynostosis mental retardation heart defects - Craniosynostosis Philadelphia type - Craniosynostosis radial aplasia syndrome - Craniosynostosis synostoses hypertensive nephropathy - Craniosynostosis Warman type - Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus - Craniosynostosis - Craniotelencephalic dysplasia -

Craw

Crawfurd syndrome -

Cre-Cro

Creatine deficiency - Creeping disease - CREST syndrome (Calcinosis Raynaud's Esophagus Sclerodactyly Telangiectasia) - Cretinism athyreotic - Cretinism - Creutzfeldt-Jakob disease - Cri du chat - Crigler-Najjar syndrome - Crisponi syndrome - Criss cross syndrome - Criswick-Schepens syndrome - Crohn's disease of the esophagus - Crohn's disease - Crome syndrome - Cronkhite-Canada disease - Crossed polydactyly type 1 - Crossed polysyndactyly - Croup - Crouzon syndrome - Crouzonodermoskeletal syndrome - Crow-Fukase syndrome -

Cry

Cryoglobulinemia - Cryophobia - Cryptococcosis - Cryptogenic organized pneumopathy - Cryptomicrotia brachydactyly syndrome excess fingers - Cryptomicrotia brachydactyly syndrome - Cryptophthalmos-syndactyly syndrome - Cryptosporidiosis - Cryptorchidism arachnodactyly mental retardation - Cryroglobulinemia - Crystal deposit disease -

Cu

Cul-Cus

Culler Jones syndrome - Curly hair ankyloblepharon nail dysplasia syndrome - Currarino triad - Curry Hall syndrome - Curth-Macklin type ichthyosis hystrix - Curtis Rogers Stevenson syndrome - Cushing syndrome, familial - Cushing's symphalangism - Cushing's syndrome -

Cut

Cutaneous anthrax - Cutaneous larva migrans - Cutaneous lupus erythematosus - Cutaneous photosensitivity colitis lethal - Cutaneous T-cell lymphoma - Cutaneous vascularitis - Cutis Gyrata syndrome of Beare and Stevenson - Cutis gyratum acanthosis nigricans craniosynostosis - Cutis laxa, recessive - Cutis laxa corneal clouding mental retardation - Cutis laxa osteoporosis - Cutis laxa with joint laxity and retarded development - Cutis laxa, dominant type - Cutis laxa, recessive type 1 - Cutis laxa, recessive type 2 - Cutis laxa - Cutis marmorata telangiectatica congenita - Cutis verticis gyrata mental deficiency - Cutis verticis gyrata thyroid aplasia mental retardation - Cutis verticis gyrata - Cutler Bass Romshe syndrome -

Cy-Cz

Cyclic neutropenia - Cyclic vomiting syndrome - Cyclosporosis - Cypress facial neuromusculoskeletal syndrome - Cystathionine beta synthetase deficiency - Cystic adenomatoid malformation of lung - Cystic angiomatosis of bone, diffuse - Cystic fibrosis gastritis megaloblastic anemia - Cystic fibrosis - Cystic hamartoma of lung and kidney - Cystic hygroma lethal cleft palate - Cystic hygroma - Cystic medial necrosis of aorta - Cystin transport, protein defect of - Cystinosis - Cystinuria - Cystinuria-lysinuria - Cytochrome C oxidase deficiency - Cytomegalic inclusion disease - Cytomegalovirus - Cytoplasmic body myopathy - Czeizel Losonci syndrome - Czeizel syndrome -

D

D ercole syndrome -

Daylon Disease

Da

Daentl Towsend Siegel syndrome - Dahlberg Borer Newcomer syndrome - Daish Hardman Lamont syndrome - Dandy Walker facial hemangioma - Dandy Walker malformation postaxial polydactyly - Dandy Walker syndrome recessive form - Dandy-walker malformation with mental retardation, basal ganglia disease, and seizures - Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy - Dandy-Walker syndrome - Daneman Davy Mancer syndrome - Darier's disease - Davenport Donlan syndrome - David syndrome - Davis Lafer syndrome - Dazippafalldown syndrome -

De

De Barsy syndrome - De Hauwere Leroy Adriaenssens syndrome - De Sanctis-Cacchione syndrome -

Dea

Deaf

Deaf blind hypopigmentation -

Deafn

Deafne

Deafness c-Deafness s

Deafness conductive ptosis skeletal anomalies - Deafness conductive stapedial ear malformation facial palsy - Deafness congenital onychodystrophy recessive - Deafness craniofacial syndrome - Deafness enamel hypoplasia nail defects - Deafness epiphyseal dysplasia short stature - Deafness goiter stippled epiphyses - Deafness hyperuricemia neurologic ataxia - Deafness hypogonadism syndrome - Deafness hypospadias metacarpal and metatarsal syndrome - Deafness mesenteric diverticula of small bowel neuropathy - Deafness mixed with perilymphatic Gusher, X-linked - Deafness nephritis ano rectal malformation - Deafness neurosensory pituitary dwarfism - Deafness nonsyndromic, Connexin 26 linked - Deafness oligodontia syndrome - Deafness onychodystrophy dominant form - Deafness peripheral neuropathy arterial disease - Deafness progressive cataract autosomal dominant - Deafness skeletal dysplasia lip granuloma - Deafness symphalangism -

Deafness v-Deafness x

Deafness vitiligo achalasia - Deafness white hair contractures papillomas - Deafness X-linked, DFN3 - Deafness, autosomal dominant nonsyndromic sensorineural - Deafness, isolated, due to mitochondrial transmission - Deafness, neurosensory nonsyndromic recessive, DFN - Deafness, X linked, DFN -

Deal

Deal Barratt Dillon syndrome -

Dec-Del

Deciduous skin - Decompensated phoria - Defect in synthesis of adenosylcobalamin - Defective apolipoprotein B-100 - Defective expression of HLA class 2 - Degenerative motor system disease - Degenerative optic myopathy - Degos disease - Degos 'en cocarde' erythrokeratoderma - Dehydratase deficiency - Dejerine-Sottas disease - Delayed membranous cranial ossification - Delayed sleep phase syndrome - Delayed speech facial asymmetry strabismus ear lobe creases - Deletion 6q16 q21 - Delleman Oorthuys syndrome - Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency - Delta-sarcoglycanopathy -

Dem-Dep

Dementia progressive lipomembranous polycysta - Dementia, familial British - Demodicidosis - Demyelinating disease - Dengue fever - Dennis Cohen syndrome - Dennis Fairhurst Moore syndrome - Dent disease - Dental aberrations steroid dehydrogenase deficienciency - Dental fluorosis - Dental tissue neoplasm - Dentatorubral pallidoluysian atrophy - Dentin dysplasia sclerotic bones - Dentin dysplasia, coronal - Dentin dysplasia, radicular - Dentinogenesis imperfecta - Dentophobia - Depersonalization disorder - Depression (clinical) -

Der-Dev

Dercum's disease aka Adiposis dolorosa - Der kaloustian Jarudi Khoury syndrome - Der Kaloustian Mcintosh Silver syndrome - Dermal Dysplasia - Dermatitis herpetiformis - Dermatocardioskeletal syndrome Boronne type - Dermatographic urticaria - Dermatofibroma - Dermatoleukodystrophy - Dermatomyositis - Dermatoosteolysis Kirghizian type - Dermatopathia pigmentosa reticularis - Dermatophytids - Dermatophytosis - Dermochondrocorneal dystrophy of François - Dermoodontodysplasia - Desbuquois syndrome - Desmin Related Myopathy - Desmoid disease - Desmoid tumor - Desmoplastic small round cell tumor - Developmental delay hypotonia extremities hypertrophy - Developmental dysphasia familial - Devic syndrome - Devriendt Legius Fryns syndrome - Devriendt Vandenberghe Fryns syndrome -

Dex

Dexamethasone sensitive hypertension - Dextrocardia with situs inversus - Dextrocardia - Dextrocardia-bronchiectasis-sinusitis -

Dg

D-glycerate dehydrogenase deficiency - D-glycericacidemia -

Di

Dia

Diab-Diam

Diabetes hypogonadism deafness mental retardation - Diabetes insipidus - Diabetes insipidus, diabetes mellitus, optic atrophy - Diabetes insipidus, nephrogenic type 1 - Diabetes insipidus, nephrogenic type 2 - Diabetes insipidus, nephrogenic type 3 - Diabetes insipidus, nephrogenic, dominant type - Diabetes insipidus, nephrogenic, recessive type - Diabetes mellitus - Diabetes mellitus, transient neonatal - Diabetes persistent mullerian ducts - Diabetes, insulin dependent - Diabetic angiopathy - Diabetic embryopathy - Diabetic nephropathy - Diabetic neuropathy - Diamond Blackfan disease -

Diap-Dias

Diaphragmatic agenesia - Diaphragmatic agenesis radial aplasia omphalocele - Diaphragmatic defect limb deficiency skull defect - Diaphragmatic hernia abnormal face limb - Diaphragmatic hernia exomphalos corpus callosum agenesis - Diaphragmatic hernia upper limb defects - Diaphragmatic hernia, congenital - Diarrhea chronic with villous atrophy - Diarrhea polyendocrinopathy infections X linked - Diastematomyelia - Diastrophic dysplasia -

Dib-Din

Dibasic aminoaciduria 2 - Dibasic aminoaciduria type 1 - Dicarboxylicaminoaciduria - Die Smulders Droog Van Dijk syndrome - Die Smulders Vles Fryns syndrome - Diencephalic syndrome - Dieterich's disease - Diethylstilbestrol antenatal infection - Diffuse idiopathic skeletal hyperostosis - Diffuse leiomyomatosis with Alport syndrome - Diffuse neonatal hemangiomatosis - Diffuse palmoplantar keratoderma, Bothnian type - Diffuse panbronchiolitis - Diffuse parenchymal lung disease - DiGeorge syndrome - Digestive duplication - Digitorenocerebral syndrome - Dihydropteridine reductase deficiency - Dihydropyrimidine dehydrogenase deficiency - Dilated cardiomyopathy - Dimitri Sturge Weber syndrome - Dincsoy Salih Patel syndrome - Dinno Shearer Weisskopf syndrome -

Dio-Dip

Diomedi Bernardi Placidi syndrome - Dionisi Vici Sabetta Gambarara syndrome - Diphallia - Diphallus rachischisis imperforate anus - Diphosphoglycerate mutase deficiency of erythrocyte - Diphtheria -

Dis-Div

Disaccharide intolerance iii - Discoid lupus erythematosus - Dislocation of the hip dysmorphism - Disorder in the hormonal synthesis with or without goiter - Disorganization syndrome - Dissecting cellulitis of the scalp - Dissociative amnesia - Dissociative hysteria - Dissociative fugue - Dissociative identity disorder - Distal arthrogryposis Moore Weaver type - Distal myopathy Markesbery-Griggs type - Distal myopathy with vocal cord weakness - Distal myopathy, Nonaka type - Distal myopathy - Distal primary acidosis, familial - Distemper - Distichiasis heart congenital anomalies - Distomatosis - Diverticulitis - Diverticulosis -

Dk-Do

Dk phocomelia syndrome - D-minus hemolytic uremic syndrome - Dobrow syndrome - Dominant cleft palate - Dominant ichthyosis vulgaris - Dominant zonular cataract - Donnai Barrow syndrome - Door syndrome - Dopamine beta-hydroxylase deficiency - DOPA-responsive dystonia - Double cortex - Double discordia - Double fingernail of fifth finger - Double outlet left ventricle - Double outlet right ventricle - Double tachycardia induced by catecholamines - Double uterus-hemivagina-renal agenesis - Downs Syndrome - Doxorubicin-induced cardiomyopathy - Doyne honeycomb retinal dystrophy -

Dp-Du

D-plus hemolytic uremic syndrome - Drachtman Weinblatt Sitarz syndrome - Dracunculiasis - Duane anomaly mental retardation - Duane syndrome - Dubin-Johnson syndrome - Dubowitz syndrome - Duchenne muscular dystrophy - Duhring Brocq disease - Duhring's disease - Duker Weiss Siber syndrome - Duodenal atresia tetralogy of Fallot - Duodenal atresia - Duplication of leg mirror foot - Duplication of the thumb unilateral biphalangeal - Duplication of urethra - Dupont Sellier Chochillon syndrome - Dupuytren subungual exostosis - Dupuytren's contracture - Dust-induced lung disease -

Dw

Dwarfism bluish sclerae - Dwarfism deafness retinitis pigmentosa - Dwarfism lethal type advanced bone age - Dwarfism mental retardation eye abnormality - Dwarfism short limb absent fibulas very short digits - Dwarfism stiff joint ocular abnormalities - Dwarfism syndesmodysplasic - Dwarfism tall vertebrae - Dwarfism thanatophoric - Dwarfism thin bones multiple fractures - Dwarfism -

Dy

Dyg-Dyk

Dyggve-Melchior-Clausen syndrome - Dykes Markes Harper syndrome -

Dys

Dysa-Dysk

Dysautonomia - Dysbarism - Dyschondrosteosis nephritis - Dyschromatosis universalis - Dysencephalia splachnocystica or Meckel Gruber - Dysequilibrium syndrome - Dyserythropoietic anemia, congenital type 1 - Dyserythropoietic anemia, congenital type 2 - Dyserythropoietic anemia, congenital type 3 - Dyserythropoietic anemia, congenital - Dysferlinopathy - Dysfibrinogenemia, familial - Dysgerminoma - Dysharmonic skeletal maturation muscular fiber disproportion - Dyskeratosis congenita of Zinsser Cole Engman - Dyskeratosis congenita - Dyskeratosis follicularis - Dyskinesia, drug induced - Dyskinesia -

Dysm-Dyss

Dysmorphism abnormal vocalization mental retardation - Dysmorphism cleft palate loose skin - Dysmorphophobia - Dysmyelination - Dysosteosclerosis - Dysostosis acral with facial and genital abnormalities - Dysostosis peripheral - Dysostosis Stanescu type - Dysostosis - Dysphasic dementia, hereditary - Dysphonia, chronic spasmodic - Dysplasia epiphysealis hemimelica - Dysplasia - Dysplastic cortical hyperostosis - Dysplastic nevus syndrome - Dysprothrombinemia - Dysraphism cleft lip palate limb reduction defects - Dyssegmental dysplasia glaucoma - Dyssegmental dysplasia Silverman Handmaker type -

Dyst

Dysthymia - Dystonia musculorum deformans type 1 - Dystonia musculorum deformans type 2 - Dystonia musculorum deformans - Dystonia progressive with diurnal variation - Dystonia - Dystrophia myotonica - Dystrophic epidermolysis bullosa - Dystrophinopathy -

Ea-Eb

EAF - Eales disease - Ear, patella, short stature syndrome - Earlobes thickened conductive deafness - Ebola hemorrhagic fever - Ebstein's anomaly -

Ec

Ecc-Ecp

Eccentrochondrodysplasia - Eccrine acrospiroma - Eclampsia - Ecp syndrome -

Ect

Ecto

Ectod

Ectode

Ectodermal dysplasia absent dermatoglyphics - Ectodermal dysplasia adrenal cyst - Ectodermal dysplasia alopecia preaxial polydactyly - Ectodermal dysplasia anhidrotic - Ectodermal dysplasia arthrogryposis diabetes mellitus - Ectodermal dysplasia Bartalos type - Ectodermal dysplasia Berlin type - Ectodermal dysplasia blindness - Ectodermal dysplasia ectrodactyly macular dystrophy - Ectodermal dysplasia hypohidrotic autosomal dominant - Ectodermal dysplasia hypohidrotic hypothyroidism ciliary dyskinesia - Ectodermal dysplasia Margarita type - Ectodermal dysplasia mental retardation CNS malformation - Ectodermal dysplasia mental retardation syndactyly - Ectodermal dysplasia neurosensory deafness - Ectodermal dysplasia osteosclerosis - Ectodermal dysplasia tricho odonto onychial type - Ectodermal dysplasia, hydrotic - Ectodermal dysplasia, hypohidrotic, autosomal recessive - Ectodermal Dysplasia - Ectodermal dysplasias - Ectodermic dysplasia anhidrotic cleft lip -

Ectop

Ectopia cordis - Ectopia lentis isolated - Ectopia pupillae - Ectopic coarctation - Ectopic ossification familial type - Ectopic pregnancy -

Ectr

Ectrodactyly cardiopathy dysmorphism - Ectrodactyly cleft palate syndrome - Ectrodactyly diaphragmatic hernia corpus callosum - Ectrodactyly dominant form - Ectrodactyly ectrodermal dysplasia - Ectrodactyly polydactyly - Ectrodactyly recessive form - Ectrodactyly - Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate - Ectropion inferior cleft lip and or palate -

Ecz

Eczema -

Ed-Eg

Edinburgh malformation syndrome - Edwards Patton Dilly syndrome - Edwards syndrome - Eec syndrome without cleft lip palate - Eec syndrome - Eem syndrome - Egg hypersensitivity - Egg shaped pupils -

Eh-Ei

Ehlers-Danlos syndrome - Ehrlichiosis - Eijkman's syndrome - Eiken syndrome - Eisenmenger syndrome -

El-Em

Elattoproteus in context of NF - Elective mutism - Ectrodactyly-ectodermal dysplasia-cleft syndrome - Electron transfer flavoprotein, deficiency of - Elejalde syndrome - Elephant man in context of NF - Elephantiasis - Elliott Ludman Teebi syndrome - Ellis Yale Winter syndrome - Ellis-Van Creveld syndrome - Emerinopathy - Emery Nelson syndrome - Emery-Dreifuss muscular dystrophy, dominant type - Emery-Dreifuss muscular dystrophy, X-linked - Emery-Dreifuss muscular dystrophy - Emetophobia - Emphysema, congenital lobar - Emphysema - Emphysema-penoscrotal web-deafness-mental retardation - Empty sella syndrome -

En

Ena-Enc

Enamel hypoplasia cataract hydrocephaly - Encephalitis - Encephalitis lethargica - Encephalo cranio cutaneous lipomatosis - Encephalocele anencephaly - Encephalocele anterior - Encephalocele frontal - Encephalocele - Encephalomyelitis, Myalgic - Encephalomyelitis - Encephalopathy intracerebral calcification retinal - Encephalopathy progressive optic atrophy - Encephalopathy subacute spongiform, Gerstmann-Stra - Encephalopathy-basal ganglia-calcification - Encephalophathy recurrent of childhood - Encephalotrigeminal angiomatosis - Enchondromatosis (benign) - Enchondromatosis dwarfism deafness - Enchondromatosis dwarfism calfness -

End-Ent

Endocardial fibroelastosis - Endocarditis, infective - Endocarditis - Endocrinopathy - Endometrial stromal sarcoma - Endometriosis - Endomyocardial fibroelastosis - Endomyocardial fibrosis - Enetophobia - Eng Strom syndrome - Engelhard Yatziv syndrome - Englemann disease - Enolase deficiency type 1 - Enolase deficiency type 2 - Enolase deficiency type 3 - Enolase deficiency type 4 - Enolase deficiency - Enterobiasis - Enteropathica - Enterovirus antenatal infection - Entomophthoramycosis -

Env

Envenomization by bothrops lanceolatus - Envenomization by the Martinique lancehead viper - Environment associated hypertension -

Eo

Eosinophilia-myalgia syndrome - Eosinophilic cryptitis - Eosinophilic cystitis - Eosinophilic fasciitis - Eosinophilic gastroenteritis - Eosinophilic granuloma - Eosinophilic lymphogranuloma - Eosinophilic Pustular Folliculitis - Eosinophilic synovitis - Eosophobia -

Ep

Epe

Ependymoblastoma - Ependymoma -

Epi

Epicondylitis -

Epid

Epide

Epidem

Epidemic encephalitis - Epidemic encephalomyelitis -

Epider

Epiderma

Epidermal nevus vitamin D resistant rickets -

Epidermo Epidermod-Epidermoi

Epidermodysplasia verruciformis - Epidermoid carcinoma -

Epidermol

Epidermolysa bullosa simplex and limb girdle muscular dystrophy - Epidermolysis bullosa acquisita - Epidermolysis bullosa dystrophica, Bart type - Epidermolysis bullosa dystrophica, dominant type - Epidermolysis bullosa herpetiformis, Dowling-Meara - Epidermolysis bullosa intraepidermic - Epidermolysis bullosa inversa dystrophica - Epidermolysis bullosa simplex with anodontia, hair - Epidermolysis bullosa simplex, Cockayne-Touraine type - Epidermolysis bullosa simplex, Koebner type - Epidermolysis bullosa simplex, Ogna type - Epidermolysis bullosa, dermolytic - Epidermolysis bullosa, generalized atrophic benign - Epidermolysis bullosa, junctional, Herlitz-Pearson - Epidermolysis bullosa, junctional, with pyloric atrophy - Epidermolysis bullosa, junctional - Epidermolysis bullosa, pretibial - Epidermolysis bullosa - Epidermolytic hyperkeratosis - Epidermolytic palmoplantar keratoderma Vorner type -

Epidi

Epididymitis -

Epil-Epis

Epilepsy benign neonatal dominant form - Epilepsy benign neonatal recessive form - Epilepsy juvenile absence - Epilepsy mental deterioration Finnish type - Epilepsy microcephaly skeletal dysplasia - Epilepsy occipital calcifications - Epilepsy progressive myoclonic type 2 - Epilepsy telangiectasia - Epilepsy with myoclono-astatic crisis - Epilepsy, benign occipital - Epilepsy, myoclonic progressive familial - Epilepsy, nocturnal, frontal lobe type - Epilepsy, partial, familial - Epilepsy - Epimerase deficiency - Epimetaphyseal dysplasia cataract - Epimetaphyseal skeletal dysplasia - Epiphyseal dysplasia dysmorphism camptodactyly - Epiphyseal dysplasia hearing loss dysmorphism - Epiphyseal dysplasia multiple - Epiphyseal stippling syndrome osteoclastic hyperplasia - Epiphysealis hemimelica dysplasia -

Epit

Epithelial-myoepithelial carcinoma - Epitheliopathy (APMPPE) - Epitheliopathy, acute posterior multifocal placoid -

Epp-Eps

EPP (erythropoietic protoporphyria) - Epstein barr virus mononucleosis - Epstein syndrome -

Eq

Equinophobia -

Er

Erb-Duchenne palsy - Erdheim disease - Erdheim–Chester disease - Ergophobia - Eronen Somer Gustafsson syndrome - Erosive pustular dermatosis of the scalp - Erysipelas - Erythema multiforme - Erythema nodosum - Erythermalgia - Erythroblastopenia - Erythroderma desquamativa of Leiner - Erythroderma lethal congenital - Erythrokeratodermia ataxia - Erythrokeratodermia progressive symmetrica ichthyosis - Erythrokeratodermia symmetrica progressiva - Erythrokeratodermia variabilis ichthyosis - Erythrokeratodermia variabilis, Mendes da Costa type - Erythrokeratodermia with ataxia - Erythrokeratolysis hiemalis ichthyosis - Erythromelalgia - Erythroplakia - Erythropoietic protoporphyria -

Es-Et

Escher Hirt syndrome - Esophageal atresia associated anomalies - Esophageal atresia coloboma talipes - Esophageal atresia - Esophageal disorder - Esophageal duodenal atresia abnormalities of hands - Esophageal neoplasm - Esophageal varices - Esotropia - Essential hypertension - Essential iris atrophy - Essential mixed cryoglobulinemia - Essential thrombocytopenia - Essential thrombocythemia - synonym of Essential thrombocytosis - Essential thrombocytosis - Esthesioneuroblastoma - Ethylmalonic aciduria - Ethylmalonic adipic aciduria -

Eu-Ew

Euhidrotic ectodermal dysplasia - Eunuchoidism familial - Evan's syndrome - Ewing's Sarcoma -

Ex-Ey

Exencephaly - Exercise induced anaphylaxis - Exfoliative dermatitis - Exner syndrome - Exogenous lipoid pneumonia - Exomphalos-macroglossia-gigantism syndrome - Exophthalmos - Exostoses anetodermia brachydactyly type E - Exostoses, multiple, type 1 - Exostoses, multiple, type 2 - Exostoses, multiple, type 3 - Exostoses, multiple - Exostoses - Experimental allergic encephalomyelitis - Exploding head syndrome - Exstrophy of the bladder - Exstrophy of the bladder-epispadias - Exudative retinopathy familial, autosomal dominant - Exudative retinopathy familial, autosomal recessive - Exudative retinopathy familial, X linked, recessive - Exudative retinopathy, familial - Extrapyramidal disorder - Extrasystoles short stature hyperpigmentation microcephaly - Eye defects arachnodactyly cardiopathy - Eyebrows duplication syndactyly -

Fa

Fab

Fabry's disease -

Fac

Face-Faci

Faces syndrome - Facial asymmetry temporal seizures - Facial clefting corpus callosum agenesis - Facial dysmorphism macrocephaly myopia Dandy Walker type - Facial dysmorphism shawl scrotum joint laxity syndrome - Facial paralysis - Facies unusual arthrogryposis advanced skeletal malformations - Facio digito genital syndrome recessive form - Facio skeletal genital syndrome Rippberger type - Facio thoraco genital syndrome - Faciocardiomelic dysplasia lethal - Faciocardiorenal syndrome - Faciooculoacousticorenal syndrome - Facioscapulohumeral muscular dystrophy -

Fact

Factor II deficiency - Factor V deficiency - Factor V Leiden mutation - Factor VII deficiency - Factor VIII deficiency - Factor X deficiency, congenital - Factor X deficiency - Factor XI deficiency, congenital - Factor XIII deficiency, congenital - Factor XIII deficiency -

Fah-Fal

Fahr's disease - Fairbank disease - Fallot tetralogy -

Fam

Fami

Famil

Famili

Familial a-Familial i

Familial ALS - Familial ALS with dementia - Familial adenomatous polyposis - Familial amyloid polyneuropathy - Familial aortic dissection - Familial band heterotopia - Familial Cold Autoinflamatory Syndrome (FCAS) - Familial Colorectal Cancer - Familial deafness - Familial dilated cardiomyopathy - Familial dysautonomia - Familial emphysema - Familial hyperchylomicronemia - Familial hyperlipoproteinemia type I - Familial hyperlipoproteinemia type III - Familial hyperlipoproteinemia type IV - Familial hyperlipoproteinemia - Familial hypersensitivity pneumonitis - Familial hypertension - Familial hypopituitarism - Familial hypothyroidism - Familial intestinal polyatresia syndrome -

Familial m-Familial w

Familial Mediterranean fever - Familial multiple lipomatosis - Familial multiple trichodiscomas - Familial myelofibrosis - Familial nasal acilia - Familial non-immune hyperthyroidism - Familial opposable triphalangeal thumbs duplication - Familial partial epilepsy with variable focus - Familial periodic paralysis - Familial polyposis - Familial porencephaly - Familial supernumerary nipples - Familial symmetric lipomatosis - Familial Treacher Collins syndrome - Familial veinous malformations - Familial ventricular tachycardia - Familial visceral myopathy - Familial wilms tumor 2 -

Fan-Faz

Fan death - Fanconi anemia type 1 - Fanconi anemia type 2 - Fanconi anemia type 3 - Fanconi Bickel syndrome - Fanconi ichthyosis dysmorphism - Fanconi like syndrome - Fanconi pancytopenia - Fanconi syndrome - Fanconi syndrome, renal, with nephrocalcinosis and renal stones - Fanconi's anemia - Fara Chlupackova syndrome - Farber's disease - Farmer's lung - Fas deficiency - Fascioliasis - Fatal familial insomnia - Fatty liver - Faulk Epstein Jones syndrome - Faye Petersen Ward Carey syndrome - Fazio Londe syndrome -

Fe

Fea-Fer

Fealty syndrome - Febrile seizure - Fechtner syndrome - Feigenbaum Bergeron Richardson syndrome - Feigenbaum Bergeron syndrome - Feingold syndrome - Felty's Syndrome - Female pseudohermaphrodism Genuardi type - Female pseudohermaphroditism - Femoral facial syndrome - Femur bifid with monodactylous ectrodactyly - Femur fibula ulna syndrome - Fenton Wilkinson Toselano syndrome - Ferlini Ragno Calzolari syndrome - Fernhoff Blackston Oakley syndrome - Ferrocalcinosis cerebro vascular -

Fet

Fetal acitretin syndrome - Fetal akinesia syndrome X linked - Fetal aminopterin syndrome - Fetal and neonatal alloimmune thrombocytopenia - Fetal antihypertensive drugs syndrome - Fetal brain disruption sequence - Fetal cytomegalovirus syndrome - Fetal diethylstilbestrol syndrome - Fetal edema - Fetal enterovirus syndrome - Fetal hydantoin syndrome - Fetal indomethacin syndrome - Fetal iodine syndrome - Fetal left ventricular aneurysm - Fetal methimazole syndrome - Fetal methyl mercury syndrome - Fetal minoxidil syndrome - Fetal parainfluenza virus type 3 syndrome - Fetal parvovirus syndrome - Fetal phenothiazine syndrome - Fetal prostaglandin syndrome - Fetal thalidomide syndrome - Fetal warfarin syndrome -

Fg

FG syndrome -

Fi

Fib-Fil

Fiber type disproportion, congenital - Fibrinogen deficiency, congenital - Fibrochondrogenesis - Fibrolipomatosis - Fibroma - Fibromatosis gingival hypertrichosis - Fibromatosis multiple non ossifying - Fibromatosis - Fibromuscular dysplasia of arteries - Fibromuscular dysplasia - Fibromyalgia - Fibrosarcoma - Fibrosing alveolitis - Fibrosing Mediastinitis - Fibrosis - Fibrous dysplasia of bone - Fibrous dysplasia - Fibrodysplasia ossificans progressiva - Fibula aplasia complex brachydactyly - Fibular aplasia ectrodactyly - Fibular hypoplasia femoral bowing oligodactyly - Fibular hypoplasia scapulo pelvic dysplasia absent - Fifth disease - Filariasis - Filippi syndrome -

Fin-Fit

Fine Lubinsky syndrome - Fingerprints absence syndactyly milia - Finnish lethal neonatal metabolic syndrome - Finnish type amyloidosis - Finucane Kurtz Scott syndrome - Fish poisoning - Fish-eye disease - Fissured tongue - Fistulous vegetative verrucous hydradenoma - Fitz-Hugh-Curtis syndrome - Fitzsimmons Walson Mellor syndrome - Fitzsimmons-Guilbert syndrome - Fitzsimmons-McLachlan-Gilbert syndrome -

Fl

Flavimonas oryzihabitans - Flesh eating bacteria - Floating limb syndrome - Floating-harbor syndrome - Florid cystic endosalpingiosis of the uterus - Flotch syndrome - Fluorosis - Flynn Aird syndrome -

Fo

Focal agyria pachygyria - Focal alopecia congenital megalencephaly - Focal dermal hypoplasia - Focal dystonia - Focal facial dermal dysplasia - Focal or multifocal malformations in neuronal migration - Foix-Chavany-Marie syndrome - Foix-Alajouanine syndrome - Follicular atrophoderma-basal cell carcinoma - Follicular Dendritic Cell Tumor - Follicular hamartoma alopecia cystic fibrosis - Follicular ichthyosis - Follicular lymphoma - Follicular lymphoreticuloma - Fontaine Farriaux Blanckaert syndrome - Forbes Albright syndrome - Forbes disease - Forestier's disease - Formaldehyde poisoning - Forney Robinson Pascoe syndrome - Fountain syndrome - Fournier gangrene - Fowler Christmas Chapele syndrome - Fox-Fordyce disease -

Fr

Fra

Fragile X syndrome type 1 - Fragile X syndrome type 2 - Fragile X syndrome type 3 - Fragile X syndrome - Fragoso Cid Garcia Hernandez syndrome - Franceschetti-Klein syndrome - Francheschini Vardeu Guala syndrome - Francois Dyscephalic Syndrome - Franek Bocker kahlen syndrome - Fraser Jequier Chen syndrome - Fraser like syndrome - Fraser syndrome - Frasier syndrome - FRAXA syndrome - FRAXD - FRAXE syndrome -

Fre-Fri

Free sialic acid storage disease - Freeman-Sheldon syndrome - Freiberg's disease - Freire Maia odontotrichomelic syndrome - Freire Maia Pinheiro Opitz syndrome - Frenkel Russe syndrome - Frey's syndrome - Frias syndrome - Fried Goldberg Mundel syndrome - Friedel Heid Grosshans syndrome - Friedman Goodman syndrome - Friedreich ataxia congenital glaucoma - Friedreich's ataxia -

Fro-Fru

Froelich's syndrome - Frölich's syndrome - Fronto nasal malformation cloacal exstrophy - Frontofacionasal dysplasia type Al gazali - Fronto-facio-nasal dysplasia - Frontometaphyseal dysplasia - Frontonasal dysplasia acromelic - Frontonasal dysplasia klippel feil syndrome - Frontonasal dysplasia phocomelic upper limbs - Frontonasal dysplasia - Frontotemporal dementia - Froster huch syndrome - Froster Iskenius Waterson syndrome - Fructose intolerance - Fructose-1,6-bisphosphatase deficiency - Fructose-1-phosphate aldolase deficiency, heredita - Fructosemia, hereditary - Fructosuria -

Fry

Frydman Cohen Ashenazi syndrome - Frydman Cohen Karmon syndrome - Fryer syndrome - Fryns Fabry Remans syndrome - Fryns Hofkens Fabry syndrome - Fryns smeets thiry syndrome -

Fu

Fucosidosis type 1 - Fucosidosis - Fuhrmann Rieger De sousa syndrome - Fukuda Miyanomae Nakata syndrome - Fukuyama type muscular dystrophy - Fumarase deficiency - Fumaric aciduria - Functioning pancreatic endocrine tumor - Fuqua Berkovitz syndrome - Furlong Kurczynski Hennessy syndrome - Furukawa Takagi Nakao syndrome - Furunculous myiasis - Fused mandibular incisors -

G

G syndrome -

Ga

Gal-Gap

Galactorrhea - Galactocoele - Galactokinase deficiency - Galactorrhoea-Hyperprolactinaemia - Galactosamine-6-sulfatase deficiency - Galactose-1-phosphate uridyltransferase deficiency - Galactosemia - Galloway Mowat syndrome - Gamborg Nielsen syndrome - Game Friedman Paradice syndrome - Gamma aminobutyric acid transaminase deficiency - Gamma-cystathionase deficiency - Gamma-sarcoglycanopathy - Gamstorp episodic adynamy - Ganglioglioma - Gangliosidosis (Type2)(GM2) - Gangliosidosis GM1 type 3 - Gangliosidosis type1 - GAPO syndrome -

Gar-Gau

Garcia Torres Guarner syndrome - Gardner Morrisson Abbot syndrome - Gardner Silengo Wachtel syndrome - Gardner-Diamond syndrome - Gardner's syndrome - Garret Tripp syndrome - Gas/bloat syndrome - Gastric Dumping Syndrome - Gastric lymphoma - Gastritis, familial giant hypertrophic - Gastrocutaneous syndrome - Gastroenteritis, eosinophilic - Gastro-enteropancreatic neuroendocrine tumor - Gastroesophageal reflux - Gastrointestinal autonomic nerve tumor - Gastrointestinal neoplasm - Gaucher disease type 1 - Gaucher disease type 2 - Gaucher disease type 3 - Gaucher Disease - Gaucher ichthyosis restrictive dermopathy - Gaucher-like disease - Gaucher's disease -

Gay

Gay Feinmesser Cohen syndrome -

Ge

Gee-Gem

Geen Sandford Davison syndrome - Gelatinous ascites - Geleophysic dwarfism - Gelineau disease - Geliphobia - Gemignani syndrome - Gemss syndrome -

Gen-Ger

Genée-Wiedemann syndrome - Generalized malformations in neuronal migration - Generalized resistance to thyroid hormone - Generalized seizure - Generalized torsion dystonia - Genes syndrome - Genetic Diseases, Inborn - Genetic reflex epilepsy - Genetic susceptibility to infections caused by BCG - Geniophobia - Genital anomaly cardiomyopathy - Genital dwarfism, Turner type - Genital dwarfism - Genito palatocardiac syndrome - Genu valgum, st. Helena familial - Genu varum - Genuphobia - Geographic tongue - German syndrome - Germinal cell aplasia - Gerodermia osteodysplastica - Gershinibaruch Leibo syndrome - Gerstmann syndrome -

Ges

Gestational diabetes mellitus - Gestational pemphigoid - Gestational trophoblastic disease -

Gh

Ghosal syndrome - Ghose Sachdev Kumar syndrome -

Gi

Gianotti-Crosti syndrome - Giant axonal neuropathy - Giant cell arteritis - Giant cell myocarditis - Giant congenital nevi - Giant ganglionic hyperplasia - Giant hypertrophic gastritis - Giant mammary hamartoma - Giant papillary conjunctivitis - Giant pigmented hairy nevus - Giant platelet syndrome - Giardiasis - Gibson's Syndrome - Giedion syndrome - Gigantism advanced bone age hoarse cry - Gigantism partial, nevi, hemihypertrophy, macrocephaly - Gigantism - Gilbert's syndrome - Gilles de la Tourette's syndrome - Gingival fibromatosis dominant - Gingival fibromatosis facial dysmorphism - Gingival fibrosis - Gingivitis - Girate atrophy of choroid and retina - Gitelman syndrome - Gittings syndrome -

Gl

Gla-Gli

Glanzmann thrombasthenia - Glass Chapman Hockley syndrome - Glaucoma ecopia microspherophakia stiff joints short stature - Glaucoma iridogoniodysgenesia - Glaucoma sleep apnea - Glaucoma type 1C - Glaucoma, congenital - Glaucoma, hereditary adult type 1A - Glaucoma, hereditary juvenile type 1B - Glaucoma, hereditary - Glaucoma, primary infantile type 3A - Glaucoma, primary infantile type 3B - Glioblastoma multiforme - Glioblastoma - Glioma - Gliomatosis cerebri - Gliosarcoma -

Glo

Globel disaccharide intolerance - Glomerulonephritis sparse hair telangiectases - Glomerulonephritis - Glomerulosclerosis - Gloomy face syndrome - Glossodynia - Glossopalatine ankylosis micrognathia ear anomalies - Glossopharyngeal neuralgia - Glossophobia -

Glu

Glucagonoma - Glucocorticoid deficiency, familial - Glucocorticoid resistance - Glucocorticoid sensitive hypertension - Glucose 6 phosphate dehydrogenase deficiency - Glucose-6-phosphate translocase deficiency - Glucose-galactose malabsorption - Glucosephosphate isomerase deficiency - Glucosidase acid-1,4-alpha deficiency - Glut2 deficiency - Glutamate decarboxylase deficiency - Glutamate-aspartate transport defect - Glutaricaciduria I - Glutaricaciduria II - Glutaryl-CoA dehydrogenase deficiency -

Gly

Glyceraldehyde-3-phosphate dehydrogenase deficiency - Glycine synthase deficiency - Glycogen storage disease - Glycogen storage disease type 1B - Glycogen storage disease type 1C - Glycogen storage disease type 1D - Glycogen storage disease type 6, due to phosphorylation - Glycogen storage disease type 7 - Glycogen storage disease type 9 - Glycogen storage disease type II - Glycogen storage disease type V - Glycogen storage disease type VI - Glycogen storage disease type VII - Glycogen storage disease type VIII - Glycogenosis type II - Glycogenosis type III - Glycogenosis type IV - Glycogenosis type V - Glycogenosis type VI - Glycogenosis type VII - Glycogenosis type VIII - Glycogenosis, type 0 - Glycosuria -

Gm

GM2 gangliosidosis, 0 variant - GM2-gangliosidosis, B, B1, AB variant - Gms syndrome -

Go

Goitre -

Gol-Gon

Goldberg Bull syndrome - Goldberg syndrome - Goldblatt Wallis syndrome - Goldblatt Wallis Zieff syndrome - Goldblatt Viljoen syndrome - Goldenhar syndrome - Goldskag Cooks Hertz syndrome - Goldstein Hutt syndrome - Gollop Coates syndrome - Gollop syndrome - Goltz syndrome - Gombo syndrome - Gomez and López-Hernández syndrome - Gonadal dysgenesis mixed - Gonadal dysgenesis Turner type - Gonadal dysgenesis XY type associated anomalies - Gonadal dysgenesis, XX type - Gonadal dysgenesis, XY female type - Gonadal dysgenesis - Goniodysgenesis mental retardation short stature - Gonococcal conjunctivitis - Gonzales Del Angel syndrome -

Goo-Gou

Goodman camptodactyly - Goodpasture pneumorenal syndrome - Goodpasture's syndrome - Gordon hyperkaliemia-hypertension syndrome - Gordon syndrome - Gorham syndrome - Gorham's disease - Gorham-Stout disease - Gorlin Bushkell Jensen syndrome - Gorlin Chaudhry Moss syndrome - Gottron's syndrome - Gougerot-Blum syndrome - Gougerot-Sjogren syndrome - Gout - Gouty nephropathy, familial -

Gr

Gra-Gri

Graft versus host disease - Graham Boyle Troxell syndrome - Grand Kaine Fulling syndrome - Grant syndrome - Granulocytopenia - Granuloma annulare - Granulomas, congenital cerebral - Granulomatosis, lymphomatoid - Granulomatous allergic angiitis - Granulomatous hypophysitis - Granulomatous rosacea - Graphite Pneumoconiosis - Graves' disease - Gray platelet syndrome - Great vessels transposition - Greenberg dysplasia - Greig cephalopolysyndactyly syndrome GCPS - Griscelli disease - Grix Blankenship Peterson syndrome -

Gro-Gru

Groll Hirschowitz syndrome - Grosse syndrome - Grover's disease - Growth deficiency brachydactyly unusual facies - Growth delay, constitutional - Growth hormone deficiency - Growth mental deficiency syndrome of Myhre - Growth retardation alopecia pseudoanodontia optic - Growth retardation hydrocephaly lung hypoplasia - Growth retardation mental retardation phalangeal hypoplasia - Grubben Decock Borghgraef syndrome -

Gt-Gy

GTP cyclohydrolase deficiency - Guanidinoacetate methyltransferase deficiency - Guérin-Stern syndrome - Guibaud Vainsel syndrome - Guillain-Barré syndrome - Guizar Vasquez Luengas syndrome - Guizar Vasquez Sanchez Manzano syndrome - Gunal Seber Basaran syndrome - Gupta Patton syndrome - Gurrieri Sammito Bellussi syndrome - Gusher syndrome - Gymnophobia - Gyrate atrophy of the retina - Gyrate atrophy -

Ha

Hag-Ham

Hageman factor deficiency - Hagemoser Weinstein Bresnick syndrome - Hailey-Hailey disease - Hair defect with photosensitivity and mental retardation - Hairy cell leukemia - Hairy ears, y-linked - Hairy ears - Hairy nose tip - Hairy palms and soles - Hairy tongue - Hajdu-Cheney syndrome - Halal Setton Wang syndrome - Halal syndrome - Hall Riggs mental retardation syndrome - Hallermann Streiff syndrome - Hallervorden-Spatz disease - Hallux valgus - Hamanishi Ueba Tsuji syndrome - Hamano Tsukamoto syndrome - Hamartoma sebaceus of Jadassohn -

Han-Hay

Hand and foot deformity flat facies - Hand foot uterus syndrome - Hand wringing Rett syndrome - Hand-foot-mouth disease - Hand-Schuller-Christian disease - Hanhart syndrome - Harding ataxia - Harlequin type ichthyosis - Harpaxophobia - Harrod Doman Keele syndrome - Hartnup disease - Hartsfield Bixler Demyer syndrome - Hashimoto struma - Hashimoto-Pritzker syndrome - Hashimoto's thyroiditis - Haspeslagh Fryns Muelenaere syndrome - Hay Wells syndrome recessive type - Hay-Wells syndrome -

He

Hea-Hei

Headache, cluster - Hearing disorder - Hearing impairment - Hearing loss - Heart aneurysm - Heart block progressive, familial - Heart block - Heart defect round face congenital retarded development - Heart defect tongue hamartoma polysyndactyly - Heart defects limb shortening - Heart hand syndrome Spanish type - Heart hypertrophy, hereditary - Heart situs anomaly - Heart tumor of the adult - Heart tumor of the child - Heavy metal poisoning - Hec syndrome - Hecht Scott syndrome - Heckenlively syndrome - Heide syndrome -

Hel

Heliophobia - HELLP syndrome - Helmerhorst Heaton Crossen syndrome - Helminthiasis -

Hem

HEM dysplasia -

Hema-Hemi

Hemangioblastoma - Hemangioendothelioma - Hemangioma thrombocytopenia syndrome - Hemangioma, capillary infantile - Hemangioma - Hemangiomatosis, familial pulmonary capillary - Hemangiopericytoma - Hemeralopia, congenital essential - Hemeralopia, familial - Hemi 3 syndrome - Hemifacial atrophy agenesis of the caudate nucleus - Hemifacial atrophy progressive - Hemifacial hyperplasia strabismus - Hemifacial microsomia - Hemihypertrophy in context of NF - Hemihypertrophy intestinal web corneal opacity - Hemimegalencephaly - Hemiplegia - Hemiplegic migraine, familial -

Hemo

Hemoglobin C disease - Hemoglobin E disease - Hemoglobin SC disease - Hemoglobinopathy - Hemoglobinuria - Hemolytic anemia lethal genital anomalies - Hemolytic-uremic syndrome - Hemophagocytic lymphohistiocytosis - Hemophagocytic reticulosis - Hemophilia A - Hemophilic arthropathy - Hemophobia - Hemorragic fever with renal syndrome - Hemorrhoid - Hemorrhagic proctocolitis - Hemorrhagic thrombocythemia - Hemorrhagiparous thrombocytic dystrophy - Hemosiderosis - Hemothorax -

Hen

Hennekam Beemer syndrome - Hennekam Koss de Geest syndrome - Hennekam syndrome - Hennekam Van der Horst syndrome -

Hep

Hepadnovirus D - Heparane sulfamidase deficiency - Heparin-induced thrombopenia - Hepatic cystic hamartoma - Hepatic ductular hypoplasia - Hepatic encephalopathy - Hepatic fibrosis renal cysts mental retardation - Hepatic fibrosis - Hepatic venoocclusive disease - Hepatic veno-occlusive disease - Hepatitis A - Hepatitis B - Hepatitis C - Hepatitis D - Hepatitis non-A non-B - Hepatitis non-A - Hepatitis non-B - Hepatitis, chronic autoimmune - Hepatitis - Hepatoblastoma - Hepatocellular carcinoma - Hepatorenal syndrome - Hepatorenal tyrosinemia -

Her

Here

Hered

Heredi

Hereditary a-Hereditary m

Hereditary amyloidosis - Hereditary angioedema - Hereditary ataxia - Hereditary carnitine deficiency myopathy - Hereditary carnitine deficiency syndrome - Hereditary carnitine deficiency - Hereditary ceroid lipofuscinosis - Hereditary coproporphyria - Hereditary deafness - Hereditary elliptocytosis - Hereditary fructose intolerance - Hereditary hearing disorder - Hereditary hearing loss - Hereditary hemochromatosis - Hereditary hemorrhagic telangiectasia - Hereditary hyperuricemia - Hereditary macrothrombocytopenia - Hereditary methemoglobinemia, recessive - Hereditary myopathy with intranuclear filamentous -

Hereditary n-Hereditary t

Hereditary nodular heterotopia - Hereditary non-spherocytic hemolytic anemia - Hereditary pancreatitis - Hereditary paroxysmal cerebral ataxia - Hereditary peripheral nervous disorder - Hereditary primary Fanconi disease - Hereditary resistance to anti-vitamin K - Hereditary sensory and autonomic neuropathy 3 - Hereditary sensory and autonomic neuropathy 4 - Hereditary sensory neuropathy type I - Hereditary sensory neuropathy type II - Hereditary spastic paraplegia - Hereditary spherocytic hemolytic anemia - Hereditary spherocytosis - Hereditary type 1 neuropathy - Hereditary type 2 neuropathy -

Herm-Hers

Hermansky-Pudlak syndrome - Hermaphroditism - Hernandez Aguire Negrete syndrome - Herpangina - Herpes encephalitis - Herpes simplex disease - Herpes simplex encephalitis - Herpes viridae disease - Herpes virus antenatal infection - Herpes zoster oticus - Herpes zoster - Herpesvirus simiae B virus - Herpetic embryopathy - Herpetic keratitis - Herpetophobia - Herrmann Opitz arthrogryposis syndrome - Herrmann Opitz craniosynostosis - Hers disease - Hersh Podruch Weisskopk syndrome -

Het-Hex

Heterophobia - Heterotaxia (generic term) - Heterotaxia autosomal dominant type - Heterotaxy with polysplenia or asplenia - Heterotaxy, visceral, X-linked - Hexosaminidases A and B deficiency -

Hh

HHH syndrome -

Hi

Histadelia - Histapenia -

Hib-Hip

Hibernian fever, familial - Hiccups - Hidradenitis suppurativa familial - Hidradenitis suppurativa - Hidrotic ectodermal dysplasia type Christianson Fouris - High scapula - High-molecular-weight kininogen deficiency, congenital - Hillig syndrome - Hing Torack Dowston syndrome - Hinson-Pepys disease - Hip dislocation - Hip dysplasia Beukes type - Hip dysplasia (canine) - Hip dysplasia (human) - Hip luxation - Hip subluxation - Hipo syndrome -

Hir-Hiv

Hirschsprung disease ganglioneuroblastoma - Hirschsprung disease polydactyly heart disease - Hirschsprung disease type 2 - Hirschsprung disease type 3 - Hirschsprung disease type d brachydactyly - Hirschsprung microcephaly cleft palate - Hirschsprung nail hypoplasia dysmorphism - Hirschsprung's disease - Hirsutism congenital gingival hyperplasia - Hirsutism skeletal dysplasia mental retardation - His bundle tachycardia - Histidinemia - Histidinuria renal tubular defect - Histiocytosis X - Histiocytosis, Non-Langerhans-Cell - Histoplasmosis - Hittner Hirsch Kreh syndrome - HIV -

Hm

Hm syndrome - HMG CoA lyase deficiency - HMG CoA synthetase deficiency -

Ho

Hod-Hol

Hodgkin lymphoma - Hodgkin's disease - Hoepffner Dreyer Reimers syndrome - Hollow visceral myopathy - Holmes Benacerraf syndrome - Holmes Borden syndrome - Holmes Collins syndrome - Holmes Gang syndrome - Holoacardius amorphus - Holocarboxylase synthetase deficiency - Holoprosencephaly caudal dysgenesis - Holoprosencephaly deletion 2p - Holoprosencephaly ectrodactyly cleft lip palate - Holoprosencephaly radial heart renal anomalies - Holoprosencephaly - Holt-Oram syndrome - Holzgreve Wagner Rehder syndrome -

Hom-Hoy

Homocarnosinase deficiency - Homocarnosinosis - Homocystinuria due to cystathionine beta-synthase - Homocystinuria due to defect in methylation (cbl g) - Homocystinuria due to defect in methylation cbl e - Homocystinuria due to defect in methylation, MTHFR deficiency - Homocystinuria - Homologous wasting disease - Homozygous hypobetalipoproteinemia - Hoon Hall syndrome - Hordnes Engebretsen Knudtson syndrome - Horn Kolb syndrome - Horner's syndrome - Hornova Dlurosova syndrome - Horseshoe kidney - Horton disease, juvenile - Horton disease - Hot tub folliculitis - Houlston Ironton Temple syndrome - Howard Young syndrome - Howell-Evans syndrome - Hoyeraal Hreidarsson syndrome - Hoyeraal syndrome -

Hs

HSV-2 infection -

Hu

Human granulocytic ehrlichiosis - Human monocytic ehrlichiosis - Human parvovirus B19 infection - Humero spinal dysostosis congenital heart disease - Humeroradial synostosis - Humeroradioulnar synostosis - Humerus trochlea aplasia of - Hunter Carpenter Mc donald syndrome - Hunter Jurenka Thompson syndrome - Hunter Macpherson syndrome - Hunter Mcalpine syndrome - Hunter Mcdonald syndrome - Hunter Rudd Hoffmann syndrome - Hunter syndrome - Huntington's disease - Huriez scleroatrophic syndrome - Hurler syndrome - Hurst Hallam Hockey syndrome - Hutchinson Gilford Progeria Syndrome - Hutchinson incisors - Hutchinson-Gilford syndrome - Hutteroth Spranger syndrome -

Hy

Hya

Hyalinosis systemic short stature - Hyaloideoretinal degeneration of wagner -

Hyd

Hyda-Hyde

Hydantoin antenatal infection - Hydatidiform mole - Hydatidosis - Hyde Forster Mccarthy Berry syndrome -

Hydr

Hydranencephaly - Hydrocephalus - Arnold Chiari - allied disorders - Hydrocephalus autosomal recessive - Hydrocephalus costovertebral dysplasia Sprengel anomaly - Hydrocephalus craniosynostosis bifid nose - Hydrocephalus endocardial fibroelastosis cataract - Hydrocephalus growth retardation skeletal anomalies - Hydrocephalus obesity hypogonadism - Hydrocephalus skeletal anomalies - Hydrocephalus - Hydrocephaly corpus callosum agenesis diaphragmatic hernia - Hydrocephaly low insertion umbilicus - Hydrocephaly tall stature joint laxity - Hydrolethalus syndrome - Hydronephrosis - Hydronephrosis peculiar facial expression - Hydrophobia - Hydrops ectrodactyly syndactyly - Hydrops fetalis anemia immune disorder absent thumb - Hydrops fetalis - Hydroxycarboxylic aciduria - Hydroxymethylglutaricaciduria -

Hyg-Hym

Hygroma cervical - Hymenolepiasis -

Hyp

Hype

Hyper

Hyper IgE - Hyper IgM syndrome -

Hypera-Hyperb

Hyperadrenalism - Hyperaldosteronism familial type 2 - Hyperaldosteronism, familial type 1 - Hyperaldosteronism - Hyperammonemia - Hyperandrogenism - Hyperbilirubinemia transient familial neonatal - Hyperbilirubinemia type 1 - Hyperbilirubinemia type 2 - Hyperbilirubinemia -

Hyperc-Hyperg

Hypercalcemia, familial benign type 1 - Hypercalcemia, familial benign type 2 - Hypercalcemia, familial benign type 3 - Hypercalcemia, familial benign - Hypercalcemia - Hypercalcinuria idiopathic - Hypercalcinuria macular coloboma - Hypercalcinuria - Hypercementosis - Hypercholesterolemia due to arg3500 mutation of Apo B-100 - Hypercholesterolemia due to LDL receptor deficiency - Hypercholesterolemia - Hyperchylomicronemia - Hypereosinophilic syndrome - Hyperexplexia - Hyperferritinemia, hereditary, with congenital cataracts - Hypergeusia - Hyperglycemia - Hyperglycerolemia - Hyperglycinemia, isolated nonketotic type 1 - Hyperglycinemia, isolated nonketotic type 2 - Hyperglycinemia, isolated nonketotic - Hyperglycinemia - Hypergonadotropic ovarian failure, familial or sporadic -

Hyperh-Hyperk

Hyperhidrosis - Hyperhomocysteinemia - Hyper-IgD syndrome - Hyperimidodipeptiduria - Hyperimmunoglobinemia D with recurrent fever - Hyperimmunoglobulin E - reccurrent infection syndrome - Hyperimmunoglobulinemia D with periodic fever - Hyperimmunoglobulinemia E - Hyperinsulinism due to focal adenomatous hyperplasia - Hyperinsulinism due to glucokinase deficiency - Hyperinsulinism due to glutamodehydrogenase deficiency - Hyperinsulinism in children, congenital - Hyperinsulinism, diffuse - Hyperinsulinism, focal - Hyperkalemia - Hyperkalemic periodic paralysis - Hyperkeratosis lenticularis perstans of Flegel - Hyperkeratosis lenticularis perstans - Hyperkeratosis palmoplantar localized acanthokeratolytic - Hyperkeratosis palmoplantar localized epidermolytic - Hyperkeratosis palmoplantar with palmar crease hyperkeratosis -

Hyperl-Hypero

Hyperlipoproteinemia type I - Hyperlipoproteinemia type II - Hyperlipoproteinemia type III - Hyperlipoproteinemia type IV - Hyperlipoproteinemia type V - Hyperlipoproteinemia - Hyperlysinemia - Hyperornithinemia - Hyperornithinemia-hyperammonemia-homocitrullinuria - Hyperostosid corticalis deformans juvenilis - Hyperostosis cortical infantile - Hyperostosis corticalis generalisata - Hyperostosis frontalis interna - Hyperoxaluria type 1 - Hyperoxaluria type 2 - Hyperoxaluria -

Hyperp-Hypers

Hyperparathyroidism, familial, primary - Hyperparathyroidism, neonatal severe primary - Hyperparathyroidism - Hyperphalangism dysmorphy bronchomalacia - Hyperphenilalaninemia due to pterin-4-alpha-carbin - Hyperphenylalalinemia due to dihydropteridine reductase deficiency - Hyperphenylalaninemia due to 6-pyruvoyltetrahydrop - Hyperphenylalaninemia due to dehydratase deficiency - Hyperphenylalaninemia due to GTP cyclohydrolase deficiency - Hyperphenylalaninemic embryopathy - Hyperpipecolatemia - Hyperprolactinemia - Hyperprolinemia type II - Hyperprolinemia - Hyperreflexia - Hyper-reninism - Hypersomnolence -

Hypert

Hyperte-Hyperth

Hypertelorism and tetralogy of Fallot - Hypertelorism hypospadias syndrome - Hypertension - Hypertensive hyperkalemia, familial - Hypertensive hypokalemia familial - Hypertensive retinopathy - Hyperthermia induced defects - Hyperthermia - Hyperthyroidism - Hyperthyroidism due to mutations in TSH receptor -

Hypertr

Hypertrichosis atrophic skin ectropion macrostomia - Hypertrichosis brachydactyly obesity and mental retardation - Hypertrichosis congenital generalized X linked - Hypertrichosis lanuginosa congenita - Hypertrichosis lanuginosa, acquired - Hypertrichosis retinopathy dysmorphism - Hypertrichosis, anterior cervical - Hypertrichotic osteochondrodysplasia - Hypertriglycidemia - Hypertrophic branchial myopathy - Hypertrophic cardiomyopathy - Hypertrophic hemangiectasia - Hypertrophic myocardiopathy - Hypertrophic osteoarthropathy, primary or idiopathic - Hypertropia - Hypertropic neuropathy of Dejerine-Sottas - Hypertryptophanemia -

Hypo

Hypoa-Hypof

Hypoadrenalism - Hypoadrenocorticism hypoparathyroidism moniliasis - Hypoaldosteronism - Hypo-alphalipoproteinemia primary - Hypobetalipoproteinaemia ataxia hearing loss - Hypobetalipoprotéinemia, familial - Hypocalcemia, autosomal dominant - Hypocalcemia - Hypocalcinuric hypercalcemia, familial type 1 - Hypocalcinuric hypercalcemia, familial type 2 - Hypocalcinuric hypercalcemia, familial type 3 - Hypocalcinuric hypercalcemia, familial - Hypochondrogenesis - Hypochondroplasia - Hypocomplementemic urticarial vasculitis - Hypodermyasis - Hypodontia dysplasia of nails - Hypodontia of incisors and premolars - Hypofibrinogenemia, familial -

Hypog-Hypol

Hypoglycemia with deficiency of glycogen synthetase in the liver - Hypoglycemia - Hypogonadism cardiomyopathy - Hypogonadism hypogonadotropic due to mutations in GR hormone - Hypogonadism male mental retardation skeletal anomaly - Hypogonadism mitral valve prolapse mental retardation - Hypogonadism primary partial alopecia - Hypogonadism retinitis pigmentosa - Hypogonadism, isolated, hypogonadotropic - Hypogonadism - Hypogonadotropic hypogonadism syndactyly - Hypogonadotropic hypogonadism without anosmia, X linked - Hypogonadotropic hypogonadism-anosmia, X linked - Hypogonadotropic hypogonadism-anosmia - Hypohidrotic Ectodermal Dysplasia - Hypokalemia - Hypokalemic alkalosis with hypercalcinuria - Hypokalemic periodic paralysis - Hypokaliemic periodic paralysis type 1 - Hypokalemic sensory overstimulation - Hypoketonemic hypoglycemia - Hypolipoproteinemia -

Hypom

Hypomagnesemia primary - Hypomandibular faciocranial dysostosis - Hypomelanotic disorder - Hypomelia mullerian duct anomalies - Hypomentia -

Hypop

Hypoparathyroidism familial isolated - Hypoparathyroidism nerve deafness nephrosis - Hypoparathyroidism short stature mental retardation - Hypoparathyroidism short stature - Hypoparathyroidism X linked - Hypoparathyroidism - Hypophosphatasia, infantile - Hypophosphatasia - Hypophosphatemic rickets - Hypopigmentation oculocerebral syndrome Cross type - Hypopituitarism micropenis cleft lip palate - Hypopituitarism postaxial polydactyly - Hypopituitarism - Hypopituitary dwarfism - Hypoplasia hepatic ductular - Hypoplasia of the tibia with polydactyly - Hypoplastic left heart syndrome - Hypoplastic right heart microcephaly - Hypoplastic thumb mullerian aplasia - Hypoplastic thumbs hydranencephaly - Hypoproconvertinemia - Hypoprothrombinemia -

Hypor-Hypox

Hyporeninemic hypoaldosteronism - Hyposmia nasal hypoplasia hypogonadism - Hypospadias familial - Hypospadias mental retardation Goldblatt type - Hyposplenism - Hypotelorism cleft palate hypospadias - Hypothalamic dysfunction - Hypothalamic hamartoblastoma syndrome - Hypothalamic hamartomas - Hypertonic Gingivitus - Hypothermia - Hypothyroidism due to iodide transport defect - Hypothyroidism postaxial polydactyly mental retardation - Hypothyroidism - Hypotonic sclerotic muscular dystrophy - Hypotrichosis mental retardation Lopes type - Hypotrichosis - Hypotropia - Hypoxanthine guanine phosphoribosyltransferase deficiency - Hypoxia -

Ib

IBIDS syndrome -

Ic

Icf

ICF syndrome -

Ich

Ichthyophobia - Ichthyosiform erythroderma corneal involvement deafness - Ichthyosis alopecia eclabion ectropion mental retardation - Ichthyosis and male hypogonadism - Ichthyosis bullosa of Siemens - Ichthyosis cheek eyebrow syndrome - Ichthyosis congenita biliary atresia - Ichthyosis deafness mental retardation skeletal anomaly - Ichthyosis follicularis atrichia photophobia syndrome - Ichthyosis hepatosplenomegaly cerebellar degeneration - Ichthyosis hystrix, Curth Macklin type - Ichthyosis linearis circumflexa - Ichthyosis male hypogonadism - Ichthyosis mental retardation Devriendt type - Ichthyosis mental retardation dwarfism renal impairment - Ichthyosis microphthalmos - Ichthyosis tapered fingers midline groove up - Ichthyosis vulgaris - Ichthyosis, erythrokeratolysis hemalis - Ichthyosis, keratosis follicularis spinulosa Decalvans - Ichthyosis, lamellar recessive - Ichthyosis, Netherton syndrome -

Id

Idaho syndrome - Idiopathic acute eosinophilic pneumonia - Idiopathic adolescent scoliosis - Idiopathic adult neutropenia - Idiopathic alveolar hypoventilation syndrome - Idiopathic congenital nystagmus, dominant, X- linked - Idiopathic diffuse interstitial fibrosis - Idiopathic dilatation of the pulmonary artery - Idiopathic dilation cardiomyopathy - Idiopathic double athetosis - Idiopathic edema - Idiopathic eosinophilic chronic pneumopathy - Idiopathic facial palsy - Idiopathic hypereosinophilic syndrome - Idiopathic infection caused by BCG or atypical mycobacteria - Idiopathic juvenile osteoporosis - Idiopathic pulmonary fibrosis - Idiopathic pulmonary haemosiderosis - Idiopathic sclerosing mesenteritis - Idiopathic thrombocytopenic purpura - Iduronate 2-sulfatase deficiency -

Ie-Im

IFAP syndrome - IgA deficiency - IGDA syndrome - Illum syndrome - Illyngophobia - Ilyina Amoashy Grygory syndrome - Imaizumi Kuroki syndrome - Iminoglycinuria - Immotile cilia syndrome, due to defective radial spokes - Immotile cilia syndrome, due to excessively long cilia - Immotile cilia syndrome, Kartagener type - Immune deficiency, familial variable - Immune thrombocytopenia - Immunodeficiency, primary - Immunodeficiency, secondary - Immunodeficiency with short limb dwarfism - Immunodeficiency, microcephaly with normal intelligence - Imperforate anus - Imperforate oropharynx costo vetebral anomalies - Impossible syndrome -

In

Ina

Inactive colon -

Inb-Ind

Inborn amino acid metabolism disorder - Inborn branched chain aminoaciduria - Inborn error of metabolism - Inborn metabolic disorder - Inborn renal aminoaciduria - Inborn urea cycle disorder - Incisors fused - Inclusion conjunctivitis - Incontinentia pigmenti type 1 - Incontinentia pigmenti type 2 - Incontinentia pigmenti - Indomethacin antenatal infection -

Inf

Infant epilepsy with migrant focal crisis - Infant respiratory distress syndrome - Infantile apnea - Infantile axonal neuropathy - Infantile convulsions and paroxysmal choreoathetosis, familial - Infantile digital fibromatosis - Infantile dysphagia - Infantile multisystem inflammatory disease - Infantile myofibromatosis - Infantile onset spinocerebellar ataxia - Infantile recurrent chronic multifocal osteomyolitis - Infantile sialic acid storage disorder - Infantile spasms broad thumbs - Infantile spasms - Infantile spinal muscular atrophy - Infantile striato thalamic degeneration - Infectious arthritis - Infectious myocarditis - Infective endocarditis - Inflammatory breast cancer - Infundibulopelvic stenosis multicystic kidney - Influenza - Inguinal hernia -

Ins

Congenital insensitivity to pain - Instability mitotic non disjunction syndrome - Insulinoma - Insulin-resistance type B - Insulin-resistant acanthosis nigricans, type A -

Int

Intercellular cholesterol esterification disease - Interferon gamma, receptor 1, deficiency - Internal carotid agenesis - Intraocular lymphoma - Interstitial cystitis - Interstitial lung disease - Interstitial pneumonia - Intestinal atresia multiple - Intestinal lipodystrophy - Intestinal lymphangiectasia - Intestinal malrotation facial anomalies familial type - Intestinal pseudoobstruction chronic idiopathic - Intestinal pseudo-obstruction - Intoeing - Intracranial aneurysms multiple congenital anomaly - Intracranial arterioveinous malformation - Intractable singultus - Intrathoracic kidney vertebral fusion - Intrauterine growth retardation mandibular malar hypoplasia - Intrauterine infections - Intrinsic factor, congenital deficiency of -

Io-Iv

Iodine antenatal infection - Iodine deficiency - Iophobia - Iridocyclitis - Iridogoniodysgenesis, dominant type - Iris dysplasia hypertelorism deafness - Iritis - Irons Bhan syndrome - Irritable bowel syndrome - Isaacs Mertens syndrome - Isaacs syndrome - Ischiadic hypoplasia renal dysfunction immunodeficiency - Ischiopatellar dysplasia - Isosporosiasis - Isotretinoin embryopathy - Isthmian coarctation - Ivemark syndrome - Ivic Syndrome -

Ja-Je

Jackson-Weiss syndrome - Jacobsen syndrome - Jadassohn Lewandowsky syndrome - Jaffer Beighton syndrome - Jalili syndrome - Jancar syndrome - Jankovic Rivera syndrome - Jansen type metaphyseal chondrodysplasia - Jansky-Bielschowsky disease - Japanese encephalitis - Jarcho-Levin syndrome - Jejunal atresia - Jensen syndrome - Jequier Kozlowski skeletal dysplasia - Jervell Lange-Nielsen syndrome - Jeune syndrome situs inversus - Jeune syndrome - Jeune asphyxiating thoracic dystrophy -

Jo

Job syndrome - Johanson Blizzard syndrome - Johnson Hall Krous syndrome - Johnson Munson syndrome - Johnston Aarons Schelley syndrome - Jones Hersh Yusk syndrome - Jones syndrome - Jorgenson Lenz syndrome - Joseph disease - Joubert syndrome bilateral chorioretinal coloboma - Joubert syndrome -

Ju

Juberg Hayward syndrome - Juberg Marsidi syndrome - Judge Misch Wright syndrome - Jumping Frenchmen of Maine - Jung Wolff Back Stahl syndrome - Juvenile cataract cerebellar atrophy myopathy mental retardation - Juvenile dermatomyositis - Juvenile gastrointestinal polyposis - Juvenile gout - Juvenile hyaline fibromatosis - Juvenile macular degeneration hypotrichosis - Juvenile muscular atrophy of the distal upper limb - Juvenile myoclonic epilepsy - Juvenile nephronophthisis - Juvenile rheumatoid arthritis - Juvenile temporal arteritis -

Ka

Kab-Kas

Kabuki syndrome - Kalam Hafeez syndrome - Kaler Garrity Stern syndrome - Kallikrein hypertension - Kallmann syndrome with Spastic paraplegia - Kallmann syndrome with heart disease - Kallmann syndrome, type 1, X linked - Kallmann syndrome, type 3, recessive - Kalyanraman syndrome - Kantaputra Gorlin syndrome - Kaolin pneumoconiosis - Kaplan Plauchu Fitch syndrome - Kaplowitz Bodurtha syndrome - Kaposi sarcoma - Kaposiform hemangio-endothelioma - Kapur Toriello syndrome - Karandikar Maria Kamble syndrome - Karsch Neugebauer syndrome - Kartagener syndrome - Kashani Strom Utley syndrome - Kasznica Carlson Coppedge syndrome -

Kat-Kaw

Kathisophobia - Katsantoni Papadakou Lagoyanni syndrome - Katz syndrome - Kaufman oculocerebrofacial syndrome - Kawasaki syndrome -

Kb

Ke

Kea-Ken

Kearns-Sayre syndrome - Keloids - Kennedy disease - Kennerknecht Sorgo Oberhoffer syndrome - Kennerknecht Vogel syndrome - Kenny Caffey syndrome - Kenny-Caffey syndrome, Type 1 -

Ker

Kera

Keratitis, hereditary - Keratoacanthoma familial - Keratoacanthoma - Keratoconjunctivitis sicca - Keratoconus posticus circumscriptus - Keratoconus - Keratoderma hypotrichosis leukonychia - Keratoderma palmoplantar deafness - Keratoderma palmoplantar spastic paralysis - Keratoderma palmoplantaris transgrediens - Keratolytic winter erythema - Keratomalacia - Keratosis focal palmoplantar gingival - Keratosis follicularis dwarfism cerebral atrophy - Keratosis follicularis spinulosa decalvans - Keratosis palmoplantaris adenocarcinoma of the colon - Keratosis palmoplantaris esophageal colon cancer - Keratosis palmoplantaris papulosa - Keratosis palmoplantaris with corneal dystrophy - Keratosis palmoplantar-periodontopathy - Keratosis pilaris - Keratosis, seborrheic -

Keri-Kern

Kerion celsi - Kernicterus -

Keu

Keutel syndrome -

Ki-Kn

Ki-1cell lymphoma - KID syndrome - Kifafa seizure disorder - Kikuchi disease - Kimura disease - King-Denborough syndrome - Kleeblattschaedel syndrome - Kleine Levin Syndrome - Kleiner Holmes syndrome - Klinefelter's Syndrome - Klippel Feil deformity conductive deafness absent vagina - Klippel Feil syndrome dominant type - Klippel Feil syndrome recessive type - Klippel Trenaunay Weber syndrome - Klippel-Feil syndrome - Klumpke paralysis - Klüver-Bucy syndrome - Kniest dysplasia - Kniest like dysplasia lethal - Knobloch-Layer syndrome - Knuckle pads, leuconychia and sensorineural deafness -

Ko

Kobberling-Dunnigan syndrome - Kocher-Debré-Semélaigne syndrome - Kohler disease - Kohlschutter Tonz syndrome - Konigsmark Knox Hussels syndrome - Koone Rizzo Elias syndrome - Korsakoff's syndrome - Korula Wilson Salomonson syndrome - Kostmann syndrome - Kosztolanyi syndrome - Kotzot-Richter syndrome - Kousseff Nichols syndrome - Kousseff syndrome - Kowarski syndrome - Kozlowski Brown Hardwick syndrome - Kozlowski Celermajer syndrome - Kozlowski Massen syndrome - Kozlowski Ouvrier syndrome - Kozlowski Rafinski Klicharska syndrome - Kozlowski Tsuruta Taki syndrome - Kozlowski Warren Fisher syndrome - Kozlowski-Krajewska syndrome -

Kr-Ky

Krabbe leukodystrophy - Krasnow Qazi syndrome - Krause-Kivlin syndrome - Krauss Herman Holmes syndrome - Krieble Bixler syndrome - Kumar Levick syndrome - Kurczynski Casperson syndrome - Kuskokwim disease - Kuster Majewski Hammerstein syndrome - Kuster syndrome - Kuzniecky syndrome - Kwashiorkor - Kyasanur forest disease - Kyphosis - Kyphosis brachyphalangy optic atrophy -

La

Lab-Lam

Labrador lung - Labyrinthitis - Lachiewicz Sibley syndrome - Lacrimo-auriculo-dento-digital syndrome - Lactate dehydrogenase deficiency type A - Lactate dehydrogenase deficiency type B - Lactate dehydrogenase deficiency type C - Lactate dehydrogenase deficiency - Lactic acidosis congenital infantile - Ladda Zonana Ramer syndrome - Lafora disease - Lagophthalmia cleft lip palate - Lambdoid synostosis familial - Lambert syndrome - Lambert-Eaton Myasthenic Syndrome (Lambert-Eaton paraneoplastic cerebellar degeneration) - Lambert-Eaton syndrome - Lamellar ichthyosis - Lamellar recessive ichthyosis -

Lan-Lap

Landau-Kleffner syndrome - Landouzy-Dejerine muscular dystrophy - Landy Donnai syndrome - Langdon Down - Langer Nishino Yamaguchi syndrome - Langer-Giedion syndrome - Langerhans cell granulomatosis - Langerhans cell histiocytosis - Laparoschisis - Laplane Fontaine Lagardere syndrome -

Lar-Lat

Large B cell diffuse lymphoma - Laron-type dwarfism - Larsen like osseous dysplasia dwarfism - Larsen like syndrome lethal type - Larsen syndrome craniosynostosis - Larsen syndrome, dominant type - Larsen syndrome, recessive type - Larsen syndrome - Laryngeal abductor paralysis mental retardation - Laryngeal carcinoma - Laryngeal cleft - Laryngeal neoplasm - Laryngeal papillomatosis - Laryngeal web congenital heart disease short stature - Laryngocele - Laryngomalacia dominant congenital - Laryngomalacia - Larynx atresia - Lassa fever - Lassueur-Graham-Little syndrome - Late onset dominant cone dystrophy - Lateral body wall defect - Laterality defects dominant - Lattice corneal dystrophy type 2 -

Lau-Lax

Launois-Bensaude adenolipomatosis - Laurence Prosser Rocker syndrome - Laurence-Moon-Bardet-Biedl syndrome - Laurin Sandrow syndrome - Laxova Brown Hogan syndrome -

Lb-Lc

LBWC - amniotic bands - LBWD syndrome - LCHAD deficiency -

Le

Lea-Leh

Leao Ribeiro Da Silva syndrome - Learman syndrome - Leber military aneurysm - Leber optic atrophy - Leber's Disease - Lecithin cholesterol acyltransferase deficiency - Ledderhose disease - Lee Root Fenske syndrome - Left ventricle-aorta tunnel - Leg absence deformity cataract - Legg-Calvé-Perthes syndrome - Legionellosis
syn: Legionnaires' disease -
- Lehman syndrome -

Lei-Ler

Leichtman Wood Rohn syndrome - Leifer Lai Buyse syndrome - Leigh disease - Leigh syndrome, French Canadian type - Leiner disease - Leiomyoma - Leiomyomatosis familial - Leiomyomatosis of oesophagus cataract hematuria - Leiomyosarcoma - Leipala Kaitila syndrome - Leishmaniasis - Leisti Hollister Rimoin syndrome - Lemierre's syndrome - Lennox-Gastaut syndrome - Lentiginosis in context of NF - Lenz Majewski hyperostotic dwarfism - Lenz microphthalmia syndrome - Leprechaunism - Leprosy - Leptomeningeal capillary - venous angiomatosis - Leptospirosis - Leri pleonosteosis - Leri-Weil syndrome -

Les-Let

Lesch-Nyhan syndrome - Lethal chondrodysplasia Moerman type - Lethal chondrodysplasia Seller type - Lethal congenital contracture syndrome - Letterer-Siwe disease -

Leu-Lev

Leucinosis - Leukemia subleukemic - Leukemia, B-Cell, chronic - Leukemia, Myeloid - Leukemia, T-Cell, chronic - Leukemia - Leukocyte adhesion deficiency syndrome - Leukocyte adhesion deficiency type 2 - Leukocytoclastic angiitis - Leukodystrophy reunion type - Leukodystrophy, globoid cell - Leukodystrophy, metachromatic - Leukodystrophy, psuedometachromatic - Leukodystrophy, Sudanophilic - Leukodystrophy - Leukoencephalopathy palmoplantar keratoderma - Leukomalacia - Leukomelanoderma mental retardation hypotrichosis - Leukoplakia - Levator syndrome - Levic Stefanovic Nikolic syndrome - Levine Crichley syndrome -

Lew-Ley

[[ -

Lg-Lh

LGCR - LGS - Lhermitte-Duclos disease -

Li

Lic-Lin

Lichen myxedematosus - Lichen planus follicularis - Lichen planus - Lichen sclerosis et atrophicus - Lichen spinulosus - Lichstenstein syndrome - Lida Kannari syndrome - Liddle syndrome - Li-Fraumeni syndrome - Light chain disease - Ligyrophobia - Limb deficiencies distal micrognathia - Limb dystonia - Limb reduction defect - Limb scalp and skull defects - Limb transversal defect cardiac anomaly - Limb-body wall complex - Limb-girdle muscular dystrophy - Lindsay Burn syndrome - Lindstrom syndrome - Linear hamartoma syndrome - Linear nevus syndrome -

Lip-Lis

Lip lit syndrome - Lipid storage myopathy - Lipidosis with triglycerid storage disease - Lipoamide dehydrogenase deficiency - Lipodystrophy Rieger anomaly diabetes - Lipodystrophy - Lipogranulomatosis - Lipoid congenital adrenal hyperplasia - Lipoid proteinosis of Urbach and Wiethe - Lipomatosis central non-encapsulated - Lipomatosis familial benign cervical - Lipomucopolysaccharidosis - Lipoprotein disorder - Liposarcoma - Lisker Garcia Ramos syndrome - Lison Kornbrut Feinstein syndrome - Lissencephaly immunodeficiency - Lissencephaly syndrome type 1 - Lissencephaly syndrome type 2 - Lissencephaly, isolated - Lissencephaly - Listeria infection - Listeriosis -

Lit-Liv

Liver cirrhosis - Liver neoplasms -

Lo

Lob-Lou

Lobar atrophy of brain - Lobster hand - Lobstein disease - Localized epiphyseal dysplasia - Locked-In syndrome - Lockwood Feingold syndrome - Loffredo Cennamo Cecio syndrome - Logic syndrome - Loiasis - Loin pain hematuria syndrome - Long QT syndrome type 1 - Long QT syndrome type 2 - Long QT syndrome type 3 - Long QT Syndrome - Loose anagen hair syndrome - Loose anagene syndrome - Lopes Gorlin syndrome - Lopes Marques de Faria syndrome - Lopez Hernandez syndrome - Lou Gehrig's disease - Louis Bar syndrome -

Low

Low birth weight dwarfism dysgammaglobulinemia - Lowe Kohn Cohen syndrome - Lowe oculocerebrorenal syndrome - Lowe syndrome - Lower limb anomaly ureteral obstruction - Lower limb deficiency hypospadias - Lower mesodermal defects - Lowry Maclean syndrome - Lowry syndrome - Lowry Wood syndrome - Lowry Yong syndrome -

Ls-Lt

LSA - L-transposition and ccTGA -

Lu

Lubani Al Saleh Teebi syndrome - Lubinsky syndrome - Lucey Driscoll syndrome - Lucky Gelehrter syndrome - Lúes Congénita - Lujan-Fryns syndrome - Lumbar malsegmentation short stature - Lundberg syndrome - Lung agenesis heart defect thumb anomalies - Lung cancer - Lung herniation congenital defect of sternem - Lung neoplasm - Lupus anticoagulant, familial - Lupus erythematosus - Lurie Kletsky syndrome - Luteinizing hormone releasing hormone, deficiency of with ataxia - Lutz Richner Landolt syndrome - Lutz-Lewandowsky epidermodysplasia verruciformis -

Ly

Lye-Lyg

Lyell's syndrome - Lygophobia -

Lym

Lyme

Lyme disease -

Lymp

Lymph

Lymph node neoplasm -

Lympha-Lymphe

Lymphadenopathy, angioimmunoblastic with dysproteinemia - Lymphangiectasies lymphoedema type Hennekam type - Lymphangiectasis - Lymphangioleiomyomatosis - Lymphangiomatosis, pulmonary - Lymphangiomyomatosis - Lymphatic filariasis - Lymphatic neoplasm - Lymphedema distichiasis - Lymphedema hereditary type 1 - Lymphedema hereditary type 2 - Lymphedema ptosis - Lymphedema, congenital - Lymphedema - Lymphedema-Distichiasis syndrome -

Lympho

Lymphoblastic lymphoma - Lymphocytes reduced or absent - Lymphocytic colitis - Lymphocytic infiltrate of Jessner - Lymphocytic vasculitis - Lymphoid hamartoma - Lymphoma, AIDS-related - Lymphoma, gastric non Hodgkins type - Lymphoma, large-cell, immunoblastic - Lymphoma, large-cell - Lymphoma, small cleaved-cell, diffuse - Lymphoma, small cleaved-cell, follicular - Lymphoma - Lymphomatoid granulomatosis - Lymphomatoid Papulosis (LyP) - Lymphomatous thyroiditis - Lymphosarcoma -

Lyn-Lys

Lynch Lee Murday syndrome - Lynch-Bushby syndrome - Lyngstadaas syndrome - LyP (lymphomatoid papulosis) - Lysine alpha-ketoglutarate reductase deficiency - Lysinuric protein intolerance - Lysosomal alpha-D-mannosidase deficiency - Lysosomal beta-mannosidase deficiency - Lysosomal disorders - Lysosomal glycogen storage disease with normal acid maltase activity -

Ma

Mac

Mac Ardle disease - Mac Dermot Patton Williams syndrome - Mac Dermot Winter syndrome -

Maci-Macr

Macias Flores Garcia Cruz Rivera syndrome - Mackay Shek Carr syndrome - Macleod Fraser syndrome - Macrocephaly cutis marmorata telangiectatica - Macrocephaly dominant type - Macrocephaly mental retardation facial dysmorphism - Macrocephaly mesodermal hamartoma spectrum - Macrocephaly mesomelic arms talipes - Macrocephaly pigmentation large hands feet - Macrocephaly short stature paraplegia - Macrodactyly of the foot - Macrodactyly of the hand - Macroepiphyseal dysplasia Mcalister Coe type - Macroglobulinemia - Macroglossia dominant - Macroglossia exomphalos gigantism - Macrogyria pseudobulbar palsy - Macrophagic myofasciitis - Macrosomia developmental delay dysmorphism - Macrosomia microphthalmia cleft palate - Macrothrombocytopenia progressive deafness - Macrothrombocytopenia with leukocyte inclusions -

Macu

Macular corneal dystrophy - Macular degeneration juvenile - Macular degeneration, age-related - Macular degeneration, polymorphic - Macular degeneration - Macular dystrophy, vitelliform - Macules hereditary congenital hypopigmented and hyperpigmented -

Mad-Mag

Mad cow disease - Madelung's disease - Madokoro Ohdo Sonoda syndrome - Maffucci syndrome - Maghazaji syndrome - Magnesium defect in renal tubular transport of - Magnesium wasting renal -

Mal

Mal de debarquement -

Mala-Mall

Malakoplakia - Malaria - Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency - Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency - Male pseudohermaphroditism due to defective LH molecule - Malformations in neuronal migration - Malignant astrocytoma - Malignant fibrous histiocytoma - Malignant germ cell tumor - Malignant hyperthermia arthrogryposis torticollis - Malignant hyperthermia susceptibility type 1 - Malignant hyperthermia susceptibility type 2 - Malignant hyperthermia susceptibility type 3 - Malignant hyperthermia susceptibility type 4 - Malignant hyperthermia susceptibility type 5 - Malignant hyperthermia susceptibility type 6 - Malignant hyperthermia - Malignant mesenchymal tumor - Malignant mixed Mullerian tumor - Malignant paroxysmal ventricular tachycardia - Mallory-Weiss syndrome -

Malo-Malp

Malonic aciduria - Malonyl-CoA decarboxylase deficiency - Malouf syndrome - Malpuech facial clefting syndrome -

Man

Mandibuloacral dysplasia - Mandibulofacial dysostosis deafness postaxial polydactyly - Manic Depression, Bipolar - Manic-depressive psychosis, genetic types - Mannosidosis - Manouvrier syndrome - Mansonelliasis - Mantle cell lymphoma -

Mar

Mara-Marg

Marashi Gorlin syndrome - Marburg fever - Marchiafava Bignami disease - Marchiafava-Micheli disease - Marcus Gunn phenomenon - Marden Walker like syndrome - Marden-Walker syndrome - Marek disease - Marfan Syndrome type II - Marfan Syndrome type III - Marfan Syndrome type IV - Marfan Syndrome type V - Marfan syndrome - Marfan-like syndrome, Boileau type - Marfan-Like syndrome - Marfanoid craniosynostosis syndrome - Marfanoid hypermobility - Marfanoid mental retardation syndrome autosomal - Marginal glioneuronal heterotopia -

Mari-Mart

Marie type ataxia - Marie Unna congenital hypotrichosis - Marinesco Sjogren like syndrome - Marinesco-Sjogren syndrome - Marion Mayers syndrome - Markel Vikkula Mulliken syndrome - Marles Greenberg Persaud syndrome - Maroteaux Cohen Solal Bonaventure syndrome - Maroteaux Fonfria syndrome - Maroteaux Le Merrer Bensahel syndrome - Maroteaux Stanescu Cousin syndrome - Maroteaux Verloes Stanescu syndrome - Maroteaux-Lamy syndrome - Marphanoid syndrome type De Silva - Marsden Nyhan Sakati syndrome - Marsden syndrome - Marshall syndrome - Marshall-Smith syndrome - Martinez Monasterio Pinheiro syndrome - Martsolf Reed Hunter syndrome - Martsolf syndrome -

Mas-May

MASA syndrome - Mass syndrome - Massa Casaer Ceulemans syndrome - Mast cell disease - Mastocytosis, short stature, hearing loss - Mastocytosis - Mastoiditis - Mastroiacovo De Rosa Satta syndrome - Mastroiacovo Gambi Segni syndrome - MAT deficiency - Maternal hyperphenylalaninemia - Maternally inherited diabetes and deafness - Mathieu De Broca Bony syndrome - Matsoukas Liarikos Giannika syndrome - Matthew-Wood syndrome - Maturity onset diabetes of the young - Maumenee syndrome - Maxillary double lip - Maxillofacial dysostosis - Maxillonasal dysplasia, Binder type - Mayer Rokitanski Kuster syndrome - May-Hegglin Anomaly -

Mc

McAlister Crane syndrome - McArdle disease - McCallum Macadam Johnston syndrome - McCune-Albright syndrome - McDonough syndrome - McDowall syndrome - McGillivray syndrome - McKusick Kaufman syndrome - McKusick type metaphyseal chondrodysplasia - McLain Debakian syndrome - McPherson Clemens syndrome - McPherson Robertson Cammarano syndrome -

Me

Mea-Med

Meacham Winn Culler syndrome - Meadows syndrome - Measles - Meckel like syndrome - Meckel syndrome - Medeira Dennis Donnai syndrome - Median cleft lip corpus callosum lipoma skin polyps - Median nodule of the upper lip - Mediastinal endodermal sinus tumors - Mediterranean fever - Medium-chain Acyl-CoA dehydrogenase deficiency - Medrano Roldan syndrome - Medullary cystic disease - Medullary thyroid carcinoma - Medulloblastoma -

Meg-Mei

Megacystis microcolon intestinal hypoperistalsis syndrome - Megaduodenum - Mega-epiphyseal dwarfism - Megalencephalic leukodystrophy - Megalencephaly-cystic leukodystrophy - Megaloblastic anemia - Megalocornea mental retardation syndrome - Megalocytic Interstitial Nephritis - Mehes syndrome - Mehta Lewis Patton syndrome - Meier Blumberg Imahorn syndrome - Meier Rotschild syndrome - Meige syndrome - Meigel disease - Meinecke Pepper syndrome - Meinecke syndrome -

Mel-Mem

Melanoma type 1 - Melanoma type 2 - Melanoma, familial - Melanoma, Malignant - Melanoma-astrocytoma syndrome - Melanosis neurocutaneous - MELAS - Meleda Disease - Melhem Fahl syndrome - Melioidosis - Melkersson-Rosenthal syndrome - Melnick-Needles osteodysplasty - Melnick-Needles syndrome - Membranoproliferative glomerulonephritis (type II) -

Men

Mend-Meno

Mendelian susceptibility to atypical mycobacteria - Menetrier's disease - Mengel Konigsmark syndrome - Ménière's disease - Meningeal angiomatosis cleft hypoplastic left heart - Meningioma 1 - Meningioma - Meningitis, meningococcal - Meningitis - Meningocele - Meningococcemia - Meningoencephalocele - Meningoencephalocele-arthrogryposis-hypoplastic thumb - Meningomyelocele -

Ment

Menta

Mental

Mental d-Mental m

Mental deficiency-epilepsy-endocrine disorders - Mental mixed retardation deafnes clubbed digits -

Mental r Mental retardation a-Mental retardation m

Mental retardation anophthalmia craniosynostosis - Mental retardation arachnodactyly hypotonia telangiectasia - Mental retardation athetosis microphthalmia - Mental retardation blepharophimosis obesity web neck - Mental retardation Buenos Aires type - Mental retardation cataracts calcified pinnae myopathy - Mental retardation coloboma slimness - Mental retardation contractural arachnodactyly - Mental retardation dysmorphism hypogonadism diabetes - Mental retardation epilepsy bulbous nose - Mental retardation epilepsy - Mental retardation gynecomastia obesity X linked - Mental retardation hip luxation G6PD variant - Mental retardation hypocupremia hypobetalipoproteinemia - Mental retardation hypotonia skin hyperpigmentation - Mental retardation macrocephaly coarse facies hypotonia - Mental retardation microcephaly phalangeal facial - Mental retardation microcephaly unusual facies - Mental retardation Mietens Weber type - Mental retardation multiple nevi - Mental retardation myopathy short stature endocrine defect - Mental retardation nasal hypoplasia obesity genital hypoplasia -

Mental retardation n-Mental retardation s

Mental retardation nasal papillomata - Mental retardation osteosclerosis - Mental retardation progressive spasticity - Mental retardation psychosis macroorchidism - Mental retardation short broad thumbs - Mental retardation short stature absent phalanges - Mental retardation short stature Bombay phenotype - Mental retardation short stature cleft palate unusual facies - Mental retardation short stature deafness genital - Mental retardation short stature hand contractures genital anomalies - Mental retardation short stature heart and skeletal anomalies - Mental retardation short stature hypertelorism - Mental retardation short stature microcephaly eye - Mental retardation short stature ocular and articular anomalies - Mental retardation short stature scoliosis - Mental retardation short stature unusual facies - Mental retardation short stature wedge shaped epiphyses - Mental retardation skeletal dysplasia abducens palsy - Mental retardation Smith Fineman Myers type - Mental retardation spasticity ectrodactyly -

Mental retardation u-Mental retardation x

Mental retardation unusual facies Ampola type - Mental retardation unusual facies Davis Lafer type - Mental retardation unusual facies talipes hand anomalies - Mental retardation unusual facies - Mental retardation Wolff type - Mental retardation X linked Atkin type - Mental retardation X linked borderline Maoa metabolism anomaly - Mental retardation X linked Brunner type - Mental retardation X linked dysmorphism - Mental retardation X linked dystonia dysarthria - Mental retardation X linked severe Gustavson type - Mental retardation X linked short stature obesity - Mental retardation X linked Tranebjaerg type seizures psoriasis - Mental retardation, unexplained - Mental retardation, X linked, Marfanoid habitus - Mental retardation, X linked, nonspecific - Mental retardation, X-linked 14 - Mental retardation - Mental retardation-polydactyly-uncombable hair -

Mer-Mes

Mercury poisoning - Meretoja syndrome - Merkle tumors - Merlob Grunebaum Reisner syndrome - Merlob syndrome - Mesangial sclerosis, diffuse - Mesenteric ischemia - Mesenteric panniculitis - Mesodermal defects lower type - Mesomelia synostoses - Mesomelia - Mesomelic dwarfism cleft palate camptodactyly - Mesomelic dwarfism Langer type - Mesomelic dwarfism Nievergelt type - Mesomelic dwarfism Reinhardt Pfeiffer type - Mesomelic dysplasia skin dimples - Mesomelic dysplasia Thai type - Mesomelic syndrome Pfeiffer type - Mesothelioma -

Met

Meta

Metabolic acidosis - Metabolic disorder - Metabolic syndrome X - Metacarpals 4 and 5 fusion - Metachondromatosis - Metageria - Metaphyseal anadysplasia - Metaphyseal chondrodysplasia Schmid type - Metaphyseal chondrodysplasia Spahr type - Metaphyseal chondrodysplasia, others - Metaphyseal dysostosis mental retardation conductive deafness - Metaphyseal dysplasia maxillary hypoplasia brachydactyly - Metaphyseal dysplasia Pyle type - Metastatic insulinoma - Metatarsus adductus - Metatrophic dysplasia - Metatropic dwarfism -

Meth

Methimazole antenatal infection - Methionine adenosyl transferase deficiency - Methyl mercury antenatal infection - Methylcobalamin deficiency cbl G type - Methylcobalamin deficiency, cbl E complementation type - Methylenetetrahydrofolate reductase deficiency - Methylmalonic acidemia with homocystinuria - Methylmalonic acidemia - Methylmalonic aciduria microcephaly cataract - Methylmalonicacidemia with homocystinuria, cbl D - Methylmalonicaciduria with homocystinuria, cbl F - Methylmalonicaciduria, vitamin B12 unresponsive, mut-0 - Methylmalonyl-Coenzyme A mutase deficiency -

Mev-Mey

Mevalonate kinase deficiency - Mevalonicaciduria - Meyenburg-Altherr-Uehlinger syndrome -

Mi

Mic

Mich-Mick

Michelin tire baby syndrome - Michels Caskey syndrome - Michels syndrome - Mickleson syndrome -

Micr

Mircre

Micrencephaly corpus callosum agenesis - Micrencephaly olivopontocerebellar hypoplasia -

Micro

Micro syndrome -

Microb

Microbrachycephaly ptosis cleft lip -

Microc

Microcephalic

Microcephalic osteodysplastic primordial dwarfism - Microcephalic primordial dwarfism Toriello type - Microcephalic primordial dwarfism -

Microcephaly Microcephaly a-Microcephaly l

Microcephaly albinism digital anomalies syndrome - Microcephaly autosomal dominant - Microcephaly brachydactyly kyphoscoliosis - Microcephaly brain defect spasticity hypernatremia - Microcephaly cardiac defect lung malsegmentation - Microcephaly cardiomyopathy - Microcephaly cervical spine fusion anomalies - Microcephaly chorioretinopathy recessive form - Microcephaly cleft palate autosomal dominant - Microcephaly deafness syndrome - Microcephaly developmental delay pancytopenia - Microcephaly facial clefting preaxial polydactyly - Microcephaly glomerulonephritis Marfanoid habitus - Microcephaly hiatus hernia nephrotic syndrome - Microcephaly hypergonadotropic hypogonadism short stature - Microcephaly immunodeficiency lymphoreticuloma - Microcephaly intracranial calcification - Microcephaly lymphoedema chorioretinal dysplasia - Microcephaly lymphoedema syndrome -

Microcephaly m-Microcephaly w

Microcephaly mental retardation retinopathy - Microcephaly mental retardation spasticity epilepsy - Microcephaly mesobrachyphalangy tracheoesophageal fistula syndrome - Microcephaly microcornea syndrome Seemanova type - Microcephaly micropenis convulsions - Microcephaly microphthalmos blindness - Microcephaly nonsyndromal - Microcephaly pontocerebellar hypoplasia dyskinesia - Microcephaly seizures mental retardation heart disorders - Microcephaly sparse hair mental retardation seizures - Microcephaly syndactyly brachymesophalangy - Microcephaly with chorioretinopathy, autosomal dominant form - Microcephaly with normal intelligence, immunodeficiency - Microcephaly with spastic quadriplegia - Microcephaly, holoprosencephaly, and intrauterine growth retardation - Microcephaly, primary autosomal recessive - Microcephaly -

Microco

Microcoria, congenital - Microcornea corectopia macular hypoplasia - Microcornea glaucoma absent frontal sinuses -

Microd-Microv

Microdontia hypodontia short stature - Microencephaly - Microgastria limb reduction defect - Microgastria short stature diabetes - Microinfarct - Micromelic dwarfism Fryns type - Micromelic dysplasia dislocation of radius - Microphtalmos bilateral colobomatous orbital cyst - Microphthalmia camptodactyly mental retardation - Microphthalmia cataract - Microphthalmia diaphragmatic hernia Fallot - Microphthalmia mental deficiency - Microphthalmia microtia fetal akinesia - Microphthalmia, Lentz type - Microphthalmia - Microphthalmos, microcornea, and sclerocornea - Microscopic polyangiitis - Microsomia hemifacial radial defects - Microspherophakia metaphyseal dysplasia - Microsporidiosis - Microtia, meatal atresia and conductive deafness - Microvillus inclusion disease -

Micu

Miculicz syndrome -

Mid-Mir

MIDAS syndrome - Midline cleft of lower lip - Midline defects autosomal type - Midline defects recessive type - Midline developmental field defects - Midline field defects - Midline lethal granuloma - Mietens syndrome - Mievis Verellen Dumoulin syndrome - Migraine - Mikulicz' Disease - Mikulicz syndrome - Miller Fisher syndrome - Miller-Dieker syndrome - Milner Khallouf Gibson syndrome - MILS syndrome - Minkowski-Chauffard disease - Minoxidil antenatal infection - Miosis, congenital - Mirror hands feet nasal defects - Mirror polydactyly segmentation and limbs defects -

Mis-Mix

Mitochondrial cytopathy (generic term) - Mitochondrial diseases of nuclear origin - Mitochondrial diseases, clinically undefinite - Mitochondrial Diseases - Mitochondrial encephalomyopathy aminoacidopathy - Mitochondrial genetic disorders - Mitochondrial myopathy lactic acidosis - Mitochondrial myopathy-encephalopathy-lactic acidosis - Mitochondrial PEPCK deficiency - Mitochondrial trifunctional protein deficiency - Mitral atresia - Mitral regurgitation deafness skeletal anomalies - Mitral valve prolapse, familial, autosomal dominant - Mitral valve prolapse, familial, X linked - Mitral valve prolapse - Miura syndrome - Mixed connective tissue disease - Mixed Müllerian tumor - Mixed sclerosing bone dystrophy -

Ml-Mn

MLS syndrome - MMEP syndrome - MMT syndrome - MN1 - MNGIE syndrome -

Mo

Mob-Mom

Mobius syndrome - MODY syndrome - Moebius axonal neuropathy hypogonadism - Moebius syndrome - Moerman Van den berghe Fryns syndrome - Moeschler Clarren syndrome - Mohr syndrome - Mohr-Tranebjaerg syndrome - Mollica Pavone Antener syndrome - Molluscum contagiosum - Moloney syndrome - Molybdenum cofactor deficiency - MOMO syndrome -

Mon-Moo

Mondini dysplasia - Mondor's disease - Monge's disease - Monilethrix - Monoamine oxidase A deficiency - Monoclonal gammopathy of undetermined significance - Monodactyly tetramelic - Mononen Karnes Senac syndrome - Mononeuritis multiplex - Monosomy 8q12 21 - Monosomy 8q21 q22 - Monosomy X - Montefiore syndrome - Moore Federman syndrome - Moore Smith Weaver syndrome -

Mor-Moy

Morel's ear - Moreno Zachai Kaufman syndrome - Morgani Turner Albright syndrome - Morhosseini Holmes Walton syndrome - Morillo Cucci Passarge syndrome - Morphea Scleroderma - Morphea, generalized - Morquio disease, type A - Morquio disease, type B - Morquio syndrome - Morrison Young syndrome - Morse Rawnsley Sargent syndrome - Motor neuron disease - Motor neuro-ophthalmic disorders - Motor neuropathy peripheral dysautonomia - Motor neuropathy - Motor sensory neuropathy type 1 aplasia cutis congenita - Mounier-Kuhn syndrome - Mount Reback syndrome - Mousa Al din Al Nassar syndrome - Moyamoya disease -

Mp-Mt

MPO deficiency - MPS III-A - MPS III-B - MPS III-C - MPS III-D - MPS VI - MRKH Syndrome (Mullerian Agenesis) - MSBD syndrome - MTHFR deficiency -

Mu

Muc-Mue

Mucha-Habermann disease - Muckle-Wells syndrome - Mucoepithelial dysplasia - Mucolipidosis type 1 - Mucolipidosis type 3 - Mucolipidosis type 4 - Mucopolysaccharidosis type 3 - Mucopolysaccharidosis type 4 - Mucopolysaccharidosis type I Hurler syndrome - Mucopolysaccharidosis type I Hurler/Scheie syndrome - Mucopolysaccharidosis type I Scheie syndrome - Mucopolysaccharidosis type II Hunter syndrome- mild form - Mucopolysaccharidosis type II Hunter syndrome- severe form - Mucopolysaccharidosis type IV-A Morquio syndrome - Mucopolysaccharidosis type IV-B - Mucopolysaccharidosis type V - Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate - Mucopolysaccharidosis type VII Sly syndrome - Mucopolysaccharidosis - Mucormycosis - Mucosulfatidosis - Muenke Syndrome -

Mul

Muli-Mull

Mulibrey Nanism syndrome - Muller Barth Menger syndrome - Mullerian agenesis - Mullerian aplasia - Mullerian derivatives lymphangiectasia polydactyly - Mullerian derivatives, persistent - Mullerian duct abnormalities galactosemia - Mulliez Roux Loterman syndrome -

Mult

Multi

Multic-Multin

Multicentric osteolysis nephropathy - Multicentric reticulohistiocytosis - Multifocal heterotopia - Multifocal motor neuropathy with conduction block - Multifocal ventricular premature beats - Multinodular goiter cystic kidney polydactyly -

Multip

Multiple a-Multiple p

Multiple acyl-CoA deficiency - Multiple carboxylase deficiency, biotin responsive - Multiple carboxylase deficiency, late onset - Multiple carboxylase deficiency, propionic acidemia - Multiple chemical sensitivity - Multiple congenital anomalies mental retardation, growth failure and cleft lip palate - Multiple congenital contractures - Multiple contracture syndrome Finnish type - Multiple endocrine neoplasia type 1 - Multiple endocrine neoplasia, type 2 - Multiple fibrofolliculoma familial - Multiple hereditary exostoses - Multiple joint dislocations metaphyseal dysplasia - Multiple myeloma - Multiple organ failure - Multiple pterygium syndrome lethal type - Multiple pterygium syndrome -

Multiple s-Multiple v

Multiple sclerosis ichthyosis factor VIII deficiency - Multiple sclerosis - Multiple subcutaneous angiolipomas - Multiple sulfatase deficiency - Multiple synostoses syndrome 1 - Multiple system atrophy - Multiple vertebral anomalies unusual facies -

Mum-Mut

Mumps - Munchausen by proxy syndrome - Muscle-eye-brain syndrome - Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus - Muscular dystrophy congenital infantile cataract hypogonadism - Muscular dystrophy congenital, merosin negative - Muscular dystrophy, facioscapulohumeral - Muscular dystrophy Hutterite type - Muscular dystrophy limb girdle type 2A, Erb type - Muscular dystrophy limb-girdle autosomal dominant - Muscular dystrophy limb-girdle type 2B, Myoshi type - Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency - Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency - Muscular dystrophy white matter spongiosis - Muscular dystrophy, congenital, merosin-positive - Muscular dystrophy, Duchenne and Becker type - Muscular dystrophy - Muscular fibrosis multifocal obstructed vessels - Muscular phosphorylase kinase deficiency - Mutations in estradiol receptor -

My

Mya-Myc

Myalgia eosinophilia associated with tryptophan - Myalgic encephalomyelitis - Myasthenia gravis congenital - Myasthenia gravis - Myasthenia, familial - Mycetoma - Mycobacterium avium complex infection - Mycoplasmal pneumonia - Mycosis fungoides lymphoma - Mycosis fungoides, familial - Mycosis fungoides - Mycositis fungoides -

Mye-Myi

Myelinopathy - Myelitis - Myelocerebellar disorder - Myelodysplasia - Myelodysplastic syndromes - Myelofibrosis, idiopathic - Myelofibrosis - Myelofibrosis-osteosclerosis - Myeloid splenomegaly - Myeloperoxidase deficiency - Myhre Ruvalcaba Graham syndrome - Myhre Ruvalcaba Kelley syndrome - Myhre School syndrome - Myhre syndrome - Myiasis -

Myo

Myoa-Myon

Myoadenylate deaminase deficiency - Myocarditis - Myocardium disorder - Myoclonic dystonia - Myoclonic progressive familial epilepsy - Myoclonus ataxia - Myoclonus cerebellar ataxia deafness - Myoclonus epilepsy partial seizure - Myoclonus epilepsy - Myoclonus hereditary progressive distal muscular atrophy - Myoclonus progressive epilepsy of Unverricht and Lundborg - Myoclonus with epilepsy with ragged red fibers (mitochondria) - Myoclonus - Myofibrillar lysis - Myofibroblastic tumors - Myoglobinuria dominant form - Myoglobinuria recurrent - Myoglobinuria - Myoneurogastrointestinal encephalopathy syndrome -

Myop

Myopathy and diabetes mellitus - Myopathy cataract hypogonadism - Myopathy congenital multicore with external ophthalmoplegia - Myopathy growth and mental retardation hypospadias - Myopathy Hutterite type - Myopathy mitochondrial cataract - Myopathy Moebius Robin syndrome - Myopathy ophthalmoplegia hypoacousia areflexia - Myopathy tubular aggregates - Myopathy with lactic acidosis and sideroblastic anemia - Myopathy with lysis of myofibrils - Myopathy, centronuclear - Myopathy, desmin storage - Myopathy, McArdle type - Myopathy, myotubular - Myopathy, X-linked, with excessive autophagy - Myopathy - Myophosphorylase deficiency - Myopia - Myopia, infantile severe - Myopia, severe - Myotubular myopathy -

Myos-Myot

Myositis ossificans post-traumatic - Myositis ossificans progressiva - Myositis ossificans - Myositis, inclusion body - Myositis - Myotonia atrophica - Myotonia mental retardation skeletal anomalies -

Myx

Myxedema - Myxoid liposarcoma - Myxoma-spotty pigmentation-endocrine overactivity - Myxomatous peritonitis - Myxozoa -

N-Nas

N acetyltransferase deficiency - N syndrome - N-acetyl glutamate synthetase deficiency - N-acetyl-alpha-D-galactosaminidase - N-acetyl-glucosamine-6-sulfate sulfatase deficiency - NADH CoQ reductase, deficiency of - NADH cytochrome B5 reductase deficiency - Naegeli syndrome - Naguib syndrome - Nail-patella syndrome - Nakajo Nishimura syndrome - Nakajo syndrome - Nakamura Osame syndrome - NAME syndrome - Nance-Horan syndrome - Nanism due to growth hormone combined deficiency - Nanism due to growth hormone isolated deficiency with X linked hypogammaglobulinemia - Nanism due to growth hormone resistance - Narcolepsy - Narcolepsy-Cataplexy - Narrow oral fissure short stature cone shaped epiphyses - Nasodigitoacoustic syndrome - Nasopalpebral lipoma coloboma syndrome - Nasopharyngeal carcinoma - Nasopharyngeal teratoma Dandy Walker diaphragmatic hernia -

Nat-Nav

Natal teeth intestinal pseudoobstruction patent ductus - Nathalie syndrome - Native American myopathy - Navajo poikiloderma - Naxos disease -

Ne

Nec-Neo

Necrotizing encephalopathy, infantile subacute - Necrotizing fasciitis - Negative rheumatoid factor polyarthritis - Neisseria meningitidis - Nelson syndrome - Nemaline myopathy - Nemaline Myopathy, Amish Type - Neonatal hemochromatosis - Neonatal hepatitis - Neonatal herpes - Neonatal ovarian cyst - Neonatal transient jaundice - Necraphilia -

Nep-Net

Nephroblastomatosis,fetal ascites,macrosomia and Wilm's tumor - Nephrocalcinosis - Nephrogenic diabetes insipidus - Nephrolithiasis type 2 - Nephronophthisis familial adult spastic quadriparesis - Nephropathy deafness hyperparathyroidism - Nephropathy familial with hyperuricemia - Nephropathy, familial with gout - Nephrosclerosis - Nephrosis deafness urinary tract digital malformation - Nephrosis neuronal dysmigration syndrome - Nephrotic syndrome - Nephrotic syndrome ocular anomalies - Nephrotic syndrome, idiopathic, steroid-resistant - Nerve sheath neoplasm - Nesidioblastosis of pancreas - Netherton syndrome ichthyosis -

Neu

Neu Laxova syndrome -

Neuh

Neuhauser Daly Magnelli syndrome - Neuhauser Eichner Opitz syndrome -

Neur

Neura-Neuri

Neural crest tumor - Neural tube defect, folate-sensitive - Neural tube defects X linked - Neuraminidase beta-galactosidase deficiency - Neuraminidase deficiency - Neurasthenia - Neurilemmomatosis - Neuritis with brachial predilection -

Neuro

Neuroa-Neurog

Neuroacanthocytosis - Neuroaxonal dystrophy renal tubular acidosis - Neuroaxonal dystrophy, late infantile - Neuroblastoma - Neurocutaneous melanosis - Neuroectodermal endocrine syndrome - Neuroectodermal tumors primitive - Neuroendocrine cancer - Neuroendocrine carcinoma of the cervix - Neuroendocrine tumor - Neuroepithelioma - Neurofaciodigitorenal syndrome - Neurofibrillary tangles - Neurofibroma - Neurofibromatosis - Neurofibromatosis type 2 - Neurofibromatosis type 3 - Neurofibromatosis type 6 - Neurofibromatosis, familial intestinal - Neurofibromatosis, Type IV, of Riccardi - Neurofibromatosis-Noonan syndrome - Neurofibrosarcoma - Neurogenic hypertension -

Neurol-Neurot

Neuroleptic malignant syndrome - Neuroma biliary tract - Neuronal heterotopia - Neuronal interstitial dysplasia - Neuronal intestinal pseudoobstruction - Neuronal intranuclear hyaline inclusion disease - Neuronal intranuclear inclusion disease - Neuropathy ataxia and retinis pigmentosa - Neuropathy congenital sensory neurotrophic keratitis - Neuropathy hereditary with liability to pressure palsies - Neuropathy motor sensory type 2 deafness mental retardation - Neuropathy sensory spastic paraplegia - Neuropathy, hereditary motor and sensory, LOM type - Neuropathy, hereditary sensory, type I - Neuropathy, hereditary sensory, type II - Neurotoxicity syndromes -

Neut

Neutral lipid storage myopathy - Neutropenia intermittent - Neutropenia monocytopenia deafness - Neutropenia, severe chronic -

Nev-Nez

Nevi flammei, familial multiple - Nevo syndrome - Nevoid basal cell carcinoma syndrome - Nevus of ota retinitis pigmentosa - Nevus sebaceus of Jadassohn - Nezelof's syndrome -

Ni

Nicolaides Baraitser syndrome - Niemann-Pick C1 disease - Niemann-Pick C2 disease - Niemann-Pick disease type C - Niemann-Pick disease type D - Niemann-Pick Disease - Night blindness skeletal anomalies unusual facies - Night blindness, congenital stationary - Nijmegen Breakage Syndrome - Nivelon Nivelon Mabille syndrome -

No

Nob-Nor

Noble Bass Sherman syndrome - Nocardiosis - Noise induced deafness - Noma - Non-24-hour sleep-wake disorder - Non functioning pancreatic endocrine tumor - Nonallergic atopic dermatitis - Non-Hodgkin lymphoma - Noninsulin-dependent diabetes mellitus with deafness - Nonketotic hyperglycinemia - Non-lissencephalic cortical dysplasia - Nonmedullary thyroid carcinoma, with cell oxyphilia - Nonne-Milroy disease - Non-small cell lung cancer - Nonsyndromic hereditary hearing impairment - Noonan like syndrome - Noonan syndrome - Norman Roberts lissencephaly syndrome - Normokalemic periodic paralysis - Norrie disease - Northern epilepsy - Norum disease -

Nos-Nov

Nose polyposis, familial - Notalgia paresthetica - Nova syndrome - Novak syndrome -

Nu-Ny

Nuchal bleb, familial - Nut Hypersensitivity - Nyctophobia -

 

O-Ob

O Doherty syndrome - O Donnell Pappas syndrome - Obesophobia - Obsessive-compulsive disorder - Obsessive-compulsive personality disorder - Obstructive asymmetric septal hypertrophy - Obstructive sleep apnea -

Oc

Occ-Och

Occipital horn syndrome - Occlusive Infantile ateriopathy - Occult spinal dysraphism - Occupational asthma - Occupational asthma - Chemicals - Occupational asthma - Metals - Occupational asthma - Plants - Occupational asthma - Wood dust - Occupational asthma - Drugs - OCD - Ochoa syndrome - Ochronosis, hereditary - Ochronosis - Ockelbo disease -

Ocu

Ocul

Ocula

Ocular Albinism - Ocular coloboma-imperforate anus - Ocular convergence spasm - Ocular Histoplasmosis - Ocular melanoma - Ocular motility disorders - Ocular toxoplasmosis -

Oculo

Oculo-auriculo-vertebral spectrum - Oculo cerebral dysplasia - Oculo cerebro acral syndrome - Oculo cerebro osseous syndrome - Oculo dento digital dysplasia - Oculo digital syndrome - Oculo facio cardio dental syndrome - Oculo skeletal renal syndrome - Oculo tricho anal syndrome - Oculo tricho dysplasia -

Oculoa-Oculog

Oculoauriculofrontonasal syndrome - Oculoauriculovertebral dysplasia - Oculocerebral hypopigmentation syndrome Cross type - Oculocerebral hypopigmentation syndrome type Preus - Oculocerebral syndrome with hypopigmentation - Oculocerebrocutaneous syndrome - Oculocerebrorenal syndrome - Oculocutaneous albinism immunodeficiency - Oculocutaneous albinism type 1 - Oculocutaneous albinism type 2 - Oculocutaneous albinism type 3 - Oculocutaneous albinism, tyrosinase negative - Oculocutaneous albinism, tyrosinase positive - Oculocutaneous tyrosinemia - Oculodental syndrome Rutherfurd syndrome - Oculodentodigital dysplasia dominant - Oculodentodigital syndrome - Oculo-dento-digital syndrome - Oculodentoosseous dysplasia dominant - Oculodentoosseous dysplasia recessive - Oculodigitoesophagoduodenal syndrome - Oculo-gastrointestinal muscular dystrophy -

Oculom-Oculor

Oculomaxillofacial dysostosis - Oculomaxillofacial dysplasia with oblique facial clefts - Oculomelic amyoplasia - Oculopalatoskeletal syndrome - Oculopharyngeal muscular dystrophy - Oculorenocerebellar syndrome -

Od-Ok

Odonto onycho dysplasia with alopecia - Odontoma - Odontomicronychial dysplasia - Odontoonychodermal dysplasia - Odontophobia - Odontotrichomelic hypohidrotic dysplasia - Odynophobia - OFD syndrome type 8 - OFD syndrome type Figuera - Ogilvie's syndrome - Ohaha syndrome - Ohdo Madokoro Sonoda syndrome - Oikophobia - Okamuto Satomura syndrome -

Ol

Olfactophobia - Oligodactyly - Oligodactyly tetramelia postaxial - Oligomeganephronic renal hypoplasia - Oligomeganephrony - Oligophernia - Oliver McFarlane syndrome - Oliver syndrome - Olivopontocerebellar atrophy deafness - Olivopontocerebellar atrophy type 1 - Olivopontocerebellar atrophy type 2 - Olivopontocerebellar atrophy type 3 - Olivopontocerebellar atrophy - Ollier disease - Olmsted syndrome -

Om-On

Ombrophobia - Omenn syndrome - Omodysplasia type 1 - Omphalocele cleft palate syndrome lethal - Omphalocele exstrophy imperforate anus - Omphalomesenteric cyst - Omsk hemorrhagic fever - Onat syndrome - Onchocerciasis - Oncocytoma - Ondine's curse - Oneirophobia - Onychonychia hypoplastic distal phalanges - Onychotrichodysplasia and neutropenia -

Op

Oph

Ophthalmic icthyosis - Ophthalmo acromelic syndrome - Ophthalmomandibulomelic dysplasia - Ophthalmophobia - Ophthalmoplegia ataxia hypoacusis - Ophthalmoplegia mental retardation lingua scrotalis - Ophthalmoplegia myalgia tubular aggregates - Opitz Mollica Sorge syndrome - Opitz Reynolds Fitzgerald syndrome - Opitz syndrome - Opportunistic infections - Oppositional defiant disorder - Opsismodysplasia -

Opt

Opthalmoplegia progressive external scoliosis - Optic atrophy opthalmoplegia ptosis deafness myopia - Optic atrophy polyneuropathy deafness - Optic atrophy, autosomal dominant - Optic atrophy, idiopathic, autosomal recessive - Optic atrophy - Optic disc drusen - Optic nerve coloboma with renal disease - Optic nerve disorder - Optic nerve hypoplasia, familial bilateral - Optic neuritis - Optic pathway glioma - Opticoacoustic nerve atrophy dementia -

Or

Ora-Orn

Oral facial digital syndrome type 3 - Oral facial digital syndrome type 4 - Oral facial digital syndrome - Oral facial dyskinesia - Oral leukoplakia - Oral lichen planus - Oral lichenoid lesions - Oral squamous cell carcinoma - Oral submucous fibrosis - Oral-facial cleft - Oral-facial-digital syndrome, type IV - Oral-facial-digital syndrome - Oral-pharyngeal disorders - Organic brain syndrome - Organic mood syndrome - Organic personality syndrome - Ornithine aminotransferase deficiency - Ornithine carbamoyl phosphate deficiency - Ornithine transcarbamylase deficiency, hyperammonemia due to - Ornithinemia - Ornithosis -

Oro-Ort

Oro acral syndrome - Orofaciodigital syndrome Gabrielli type - Orofaciodigital syndrome Shashi type - Orofaciodigital syndrome Thurston type - Orofaciodigital syndrome type 2 - Orofaciodigital syndrome type1 - Orotic aciduria hereditary - Orotic aciduria purines-pyrimidines - Orotidylic decarboxylase deficiency - Orstavik Lindemann Solberg syndrome - Orthostatic intolerance -

Os

Ose-Oss

Osebold Remondini syndrome - Osgood-Schlatter disease - Oslam syndrome - Osmed Syndrome - Ossicular Malformations, familial -

Ost

Oste

Ostei

Osteitis deformans -

Osteo

osteo: bone

Osteoa-Osteom

Osteoarthritis - Osteoarthropathy of fingers familial - Osteochondritis deformans juvenile - Osteochondritis dissecans - Osteochondritis - Osteochondrodysplasia thrombocytopenia hydrocephalus - Osteochondroma - Osteocraniostenosis - Osteodysplasia familial Anderson type - Osteodysplastic dwarfism Corsello type - Osteoectasia familial - Osteogenesis Imperfecta - Osteogenesis imperfecta congenita microcephaly and cataracts - Osteogenesis imperfecta congenital joint contractures - Osteogenesis imperfecta retinopathy - Osteogenic sarcoma - Osteoglophonic dwarfism - Osteolysis hereditary multicentric - Osteolysis syndrome recessive - Osteomalacia - Osteomyelitis -

Osteon-Osteos

Osteonecrosis - Osteopathia condensans disseminata with osteopoikilosis - Osteopathia striata cranial sclerosis - Osteopathia striata pigmentary dermopathy white forelock - Osteopetrosis autosomal dominant type 1 - Osteopetrosis lethal - Osteopetrosis renal tubular acidosis - Osteopetrosis, (generic term) - Osteopetrosis, malignant - Osteopetrosis, mild autosomal recessive form - Osteopoikilosis - Osteoporosis macrocephaly mental retardation blindness - Osteoporosis oculocutaneous hypopigmentation syndrome - Osteoporosis pseudoglioma syndrome - Osteoporosis - Osteosarcoma limb anomalies erythroid macrocytosis - Osteosclerose type Stanescu - Osteosclerosis abnormalities of nervous system and meninges - Osteosclerosis autosomal dominant Worth type - Osteosclerosis -

Oster

Ostertag type amyloidosis -

Ot-Ox

Ota Appaura syndrome - Ota Kawamura Ito syndrome - Oto palato digital syndrome type I and II - Otodental dysplasia - Otofaciocervical syndrome - Otoonychoperoneal syndrome - Oto-Palatal-digital syndrome - Otopalatodigital syndrome type 2 - Otosclerosis, familial - Otosclerosis - Otospondylomegaepiphyseal dysplasia - Ouvrier Billson syndrome - Ovarian cancer - Ovarian carcinosarcoma - Ovarian dwarfism as part of Turner Syndrome - Ovarian dwarfism - Ovarian insufficiency due to FSH resistance - ovarian remnant syndrome - Overfolded helix - Overgrowth radial ray defect arthrogryposis - Overgrowth syndrome type Fryer - Overhydrated hereditary stomatocytosis - Overwhelming post-splenectomy infection (OPSI) - Oxalosis -

Pa

Pac-Pal

Pachydermoperiostosis - Pachygyria - Pachyonychia congenita Jackson Lawler type - Pacman dysplasia - Paes Whelan Modi syndrome - Paget disease extramammary - Paget disease juvenile type - Paget's disease of bone - Paget's disease of the breast - Paget's disease, type 1 - Pagon Bird Detter syndrome - Pagon Stephan syndrome - Pai Levkoff syndrome - Palant cleft palate syndrome - Palindromic rheumatism - Pallister-Hall syndrome - Pallister-Killian syndrome - Palmer Pagon syndrome - Palmitoyl-protein thioesterase deficiency - Palmoplantar Keratoderma - Palmoplantar porokeratosis of Mantoux - Palsy cerebral -

Pan

Pancreas agenesis - Pancreas divisum - Pancreatic adenoma - Pancreatic beta cell agenesis with neonatal diabetes mellitus - Pancreatic cancer - Pancreatic carcinoma, familial - Pancreatic diseases - Pancreatic islet cell neoplasm - Pancreatic islet cell tumors - Pancreatic lipomatosis duodenal stenosis - Pancreatitis, hereditary - Pancreatoblastoma - PANDAS - Panhypopituitarism - Panic disorder - Panmyelophthisis aplastic anemia - Panniculitis - Panophobia - Panostotic fibrous dysplasia - Panthophobia -

Pap

Papilledema - Papillion-Lefevre syndrome - Papillitis - Papilloma of choroid plexus - Papular mucinosis - Papular urticaria -

Par

Para-Pari

Paracoccidioidomycosis - Paraganglioma - Parainfluenza virus type 3 antenatal infection - Paramyotonia congenita of von Eulenburg - Paramyotonia congenita - Paraneoplastic cerebellar degeneration - Paraomphalocele - Paraparesis amyotrophy of hands and feet - Paraphilia - Paraplegia - Paraplegia-brachydactyly-cone shaped epiphysis - Paraplegia-mental retardation-hyperkeratosis - Parapsoriasis - Parasitophobia - Parastremmatic dwarfism - Parathyroid cancer - Parathyroid neoplasm - Paratyphoid fever - PARC syndrome - Parcopresis Spongebob - Parenchymatous cortical degeneration of cerebellum - Paris-Trousseau thrombopenia -

Park-Parv

Parkes-Weber syndrome - Parkinson's disease - Parkinson dementia Steele type - Parkinsonism early onset mental retardation - Parkinsonism - Parkinson's disease - Paroxysmal cold hemoglobinuria - Paroxysmal dystonic choreoathetosis - Paroxysmal nocturnal hemoglobinuria - Paroxysmal ventricular fibrillation - Parry-Romberg syndrome - Pars planitis - Parsonage Turner syndrome - Partial agenesis of corpus callosum - Partial atrioventricular canal - Partial deletion of Y - Partial gigantism in context of NF - Partial lissencephaly - Partington Anderson syndrome - Partington Mulley syndrome - Parturiphobia - Paruresis - Parvovirus antenatal infection -

Pas-Pat

Pascuel Castroviejo syndrome - Pashayan syndrome - Pat1 - Pat11 - Pat111 - Pat12 - Pat121 - Pat13 - Pat131 - Pat132 - Pat14 - Pat141 - Pat142 - Patau syndrome - Patel Bixler syndrome - Patella aplasia, coxa vara, tarsal synostosis - Patella hypoplasia mental retardation - Patent ductus arteriosus familial - Patent ductus arteriosus - Patterson Lowry syndrome - Patterson pseudoleprechaunism syndrome - Patterson Stevenson syndrome -

Pau-Pav

Pauciarticular chronic arthritis - Pavone Fiumara Rizzo syndrome -

Pe

Pea-Pem

Peanut hypersensitivity - Pearson's marrow/pancreas syndrome - Pediatric T-cell leukemia - Pediculosis - Peeling skin syndrome ichthyosis - PEHO syndrome - Pelizaeus-Merzbacher brain sclerosis - Pelizaeus-Merzbacher disease, recessive, acute infantile - Pelizaeus-Merzbacher disease - Pelizaeus-Merzbacher leukodystrophy - Pellagra like syndrome - Pellagrophobia - Pelvic dysplasia arthrogryposis of lower limbs - Pelvic inflammatory disease - Pelvic lipomatosis - Pelvic shoulder dysplasia - Pemphigus and fogo selvagem - Pemphigus foliaceus - Pemphigus vulgaris, familial - Pemphigus vulgaris - Pemphigus -

Pen-Pep

Pena Shokeir syndrome - Pendred syndrome - Penis agenesia - Penoscrotal transposition - Penta X syndrome - Pentalogy of Cantrell - Pentosuria - Penttinen-Aula syndrome - PEPCK 1 deficiency - PEPCK 2 deficiency - PEPCK deficiency, mitochondrial - Peptidic growth factors deficiency -

Per

Perceptual disorder - Processing disorder -

Peri

Periarteritis nodosa - Pericardial constriction with growth failure - Pericardial defect diaphragmatic hernia - Pericardium absent mental retardation short stature - Pericardium congenital anomaly - Perilymphatic fistula - Perimyositis - Perinatal infections - Periodic disease - Periodic fever, aphthous stomatitis, pharyngitis and adenitis - Periodontal disease / Periodontitis - Peripartum cardiomyopathy - Peripheral blood vessel disorder - Peripheral nervous disorder - Peripheral neuroectodermal tumor - Peripheral neuropathy - Peripheral T-cell lymphoma - Peripheral type neurofibromatosis - Perisylvian syndrome - Peritonitis - Periventricular laminar heterotopia - Periventricular leukomalacia -

Pern-Pert

Pernicious anemia - Perniola Krajewska Carnevale syndrome - Perniosis - Peroxisomal Bifunctional Enzyme Deficiency - Peroxisomal defects - Persistent Mullerian duct syndrome (PMDS) - Persistent parvovirus infection - Persistent sexual arousal syndrome - Persistent truncus arteriosus - Pertussis -

Pes-Pey

Pes planus - Peters anomaly with cataract - Peters anomaly - Peters congenital glaucoma - Petit Fryns syndrome - Petty Laxova Wiedemann syndrome - Peutz-Jeghers syndrome - Peyronie disease -

Pf

Pfeiffer cardiocranial syndrome - Pfeiffer Hirschfelder Rott syndrome - Pfeiffer Kapferer syndrome - Pfeiffer Mayer syndrome - Pfeiffer Palm Teller syndrome - Pfeiffer Rockelein syndrome - Pfeiffer Singer Zschi