All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02307 - adenome, pituitary (prolactinoma, familial) 600634 - - - AIP - -
06690 AIFBL1 autoinflammatory syndrome, familial, Behcet-like, type 1 616744 AD - - TNFAIP3 - -
02508 LCA4 Leber congenital amaurosis, type 4 (LCA4) 604393 AD;AR 11 11 AIPL1 - -
05265 MRRSDC;LGMD2Y dystrophy, dystrophy, autosomal recessive, with rigid spine and distal joint contractures (LGMD2Y) 617072 AR 1 1 TOR1AIP1 - -
01044 PAGH1 pituitary adenoma, type 1, multiple types (PITA1) 102200 AD;SMu - - AIP, GNAS, SSTR5 - -
01731 PITA4 adenoma, pituitary, ACTH-secreting, type 4 219090 - - - AIP - -
06556 SCKL9 Seckel syndrome, type 9 616777 AR - - TRAIP - -
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