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Summary Literature (0)
MIM:610600 - CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY

Xenbase Genes: cyp11b2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012524 - corticosterone methyloxidase type 2 deficiency
MONDO:0018541 - familial hypoaldosteronism
MONDO:0020489 - obsolete familial hyperreninemic hypoaldosteronism type 1