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Summary Literature (0)
MIM:202110 - ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY

Xenbase Genes: cyp17a1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008730 - congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
MONDO:0018479 - congenital adrenal hyperplasia
MONDO:0019597 - obsolete 46,XY disorder of sex development due to isolated 17,20-lyase deficiency

Disease Ontology (DO):
DOID:0050811 - congenital adrenal hyperplasia