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
01630 - steroid 11-beta-monooxygenase deficiency 202010 AR 1 - CYP11B1 - -
01168 HALD1;GRA hyperaldosteronism, glucocorticoid-remediable (HALD1) 103900 AD - - CYP11B1 - -
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