Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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 - kidney corticomedullary boundary
MONDO:0019161 - pseudohypoaldosteronism type 1

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