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Summary Literature (1)
MIM:264350 - PSEUDOHYPOALDOSTERONISM, TYPE IB1, AUTOSOMAL RECESSIVE; PHA1B1

Xenbase Genes: scnn1b, scnn1g, scnn1a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009917 - pseudohypoaldosteronism, type IB1, autosomal recessive
MONDO:0019161 - pseudohypoaldosteronism type 1

Disease Ontology (DO):
DOID:0060854 - autosomal recessive pseudohypoaldosteronism type 1