|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Congenital adrenal hyperplasia due to 11 beta-hydroxylase (CYP11B1) deficiency is a rare form of congenital adrenal hyperplasia (CAH; see this term) characterized by glucocorticoid deficiency, hyperandrogenism, hypertension and virilization in females. (Orphanet Rare Disease Ontology, Orphanet_90795)|
|Downloads & Tools|
1 genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
|CYP11B1||cytochrome P450, family 11, subfamily B, polypeptide 1||2.88009|