Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535978
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Genes

1 genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1 2.88009