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
02139 AIS insensitivity syndrome, androgen (AIS) 300068 XLR 590 590 AR, FOXD3 - -
02712 AIS1 autoimmune disease, susceptibility to, type 1 (AIS-1) 607836 AD - - FOXD3 - -
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