All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00150 IDDM diabetes mellitus, insulin-dependent (IDDM) 222100 - 8 8 FOXP3, HNF1A, IL6, INS, ITPR3, OAS1, PTPN22 - -
02231 IPEX immunodysregulation, polyendocrinopathy, and enteropathy, X-linked (IPEX) 304790 - 0 0 FOXP3 - an X-linked recessive immunologic disorder characterized by onset in infancy of severe diarrhea due to enteropathy, type 1 diabetes mellitus, and dermatitis; other features may include hypothyroidism, autoimmune hemolytic anemia, thrombocytopenia, lymphadenopathy, hepatitis, nephritis
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