All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01629 adrenal hyperplasia adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 201910 AR 32 29 CYP21A2, TNXB - -
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