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Summary Literature (0)
MIM:201910 - ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

Xenbase Genes: cyp21a2.1, cyp21a2.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008728 - classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
MONDO:0018479 - congenital adrenal hyperplasia

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