17-alpha-hydroxylase/17,20-lyase deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/202110
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Genes

1 genes associated with the 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1