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
00089 CH Congenital hypothyroidism - - 20 2 FOXE1, TPO, TSHR - -
00088 TDH Thyroid Dyshormonogenesis - - - - TPO - -
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