Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535979
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP21A2 cytochrome P450, family 21, subfamily A, polypeptide 2 2.88009