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MIM:264350 - PSEUDOHYPOALDOSTERONISM, TYPE IB1, AUTOSOMAL RECESSIVE; PHA1B1
Xenbase Genes: scnn1b, scnn1g, scnn1a
Human Disease Resource: OMIM
MONDO:0009917 - autosomal recessive pseudohypoaldosteronism type 1 |
MONDO:0019161 - pseudohypoaldosteronism type 1 |
DOID:0060854 - autosomal recessive pseudohypoaldosteronism type 1 |