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
01637 - corticosterone methyloxidase type 1 deficiency 203400 AR 5 - CYP11B2 - -
02961 - Hypoaldosteronism, congenital, due to CMO II deficiency 610600 AR 3 - CYP11B2 - -
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