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Summary Literature (1)
MIM:177735 - PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A

Xenbase Genes: nr3c2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008329 - autosomal dominant pseudohypoaldosteronism type 1
MONDO:0019161 - pseudohypoaldosteronism type 1

Disease Ontology (DO):
DOID:0060855 - autosomal dominant pseudohypoaldosteronism type 1