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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342]
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C17. Skin and Connective Tissue Diseases: Skin Diseases [MESH:D012871] > Hair Diseases [MESH:D006201] > Hypotrichosis [MESH:D007039] > Alopecia [MESH:D000505] > Alopecia Areata [MESH:D000506]
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The current query selects 160 items in 56 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Genetic Diseases, Inborn [MESH:D030342]" below.

Subcategories in C16. Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342]:
(jump to A - B - C - D - E - F - G - H - K - L - M - N - O - P - S - W - Y)
- A -
ACTH Deficiency, Isolated [MESH:C562707] (21)
Adrenal Hyperplasia, Congenital [MESH:D000312] (74)
Alagille Syndrome [MESH:D016738] (35)
Anemia, Hemolytic, Congenital [MESH:D000745] (127)
Anemia, Hypoplastic, Congenital [MESH:D029502] (122)
Angioedemas, Hereditary [MESH:D054179] (38)
Ataxia Telangiectasia [MESH:D001260] (34)
Atrial Standstill [MESH:C563984] (12)
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (95)
alpha 1-Antitrypsin Deficiency [MESH:D019896] (21)
 
- B -
Blood Coagulation Disorders, Inherited [MESH:D025861] (86)
Brugada Syndrome [MESH:D053840] (43)
 
- C -
CADASIL [MESH:D046589] (16)
CHARGE Syndrome [MESH:D058747] (10)
Camurati-Engelmann Syndrome [MESH:D003966] (78)
Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (75)
Cherubism [MESH:D002636] (11)
Chromosome Disorders [MESH:D025063] (123)
Cirrhosis, Familial [MESH:C566123] (46)
Complement Factor I Deficiency [MESH:C572568] (21)
Corticosteroid-Binding Globulin Deficiency [MESH:C565152] (18)
Costello Syndrome [MESH:D056685] (72)
Cystic Fibrosis [MESH:D003550] (93)
 
- D -
Donohue Syndrome [MESH:D056731] (27)
Dwarfism [MESH:D004392] (86)
 
- E -
Eye Diseases, Hereditary [MESH:D015785] (129)
 
- F -
Frasier Syndrome [MESH:D052159] (20)
 
- G -
Genetic Diseases, X-Linked [MESH:D040181] (145)
Genetic Diseases, Y-Linked [MESH:D050174] (1)
 
 - H -
Hajdu-Cheney Syndrome [MESH:D031845] (19)
Hemoglobinopathies [MESH:D006453] (124)
Hereditary Autoinflammatory Diseases [MESH:D056660] (60)
Hereditary Myopathy with Early Respiratory Failure [MESH:C566343] (14)
Heredodegenerative Disorders, Nervous System [MESH:D020271] (152)
Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (50)
 
- K -
Kallmann Syndrome [MESH:D017436] (42)
Kartagener Syndrome [MESH:D007619] (14)
 
- L -
Loeys-Dietz Syndrome [MESH:D055947] (61)
 
- M -
Marfan Syndrome [MESH:D008382] (84)
Metabolism, Inborn Errors [MESH:D008661] (158)
Muscular Dystrophies [MESH:D009136] (129)
Myasthenic Syndromes, Congenital [MESH:D020294] (41)
 
- N -
Nail-Patella Syndrome [MESH:D009261] (2)
Neoplastic Syndromes, Hereditary [MESH:D009386] (139)
 
- O -
Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (27)
Osteogenesis Imperfecta [MESH:D010013] (77)
 
- P -
Pain Insensitivity, Congenital [MESH:D000699] (8)
Pelger-Huet Anomaly [MESH:D010381] (19)
Platelet Glycoprotein IV Deficiency [MESH:C564245] (48)
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (69)
Pulmonary Alveolar Microlithiasis [MESH:C562405] (13)
Pycnodysostosis [MESH:D058631] (19)
 
- S -
Skin Diseases, Genetic [MESH:D012873] (141)
 
- W -
Weill-Marchesani Syndrome [MESH:D056846] (26)
Werner Syndrome [MESH:D014898] (32)
 
- Y -
Yellow Nail Syndrome [MESH:D056684] (11)