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Summary Literature (1)
OMIM:264350 - PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B


Xenbase Genes: scnn1b, scnn1g, scnn1a

Human Disease Resource: OMIM

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

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