|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050546)|
|Downloads & Tools|
1 genes associated with the adrenal insufficiency, congenital, with 46xy sex reversal, partial or complete phenotype from the curated OMIM Gene-Disease Associations dataset.
|CYP11A1||cytochrome P450, family 11, subfamily A, polypeptide 1|