Term Name:	autosomal dominant pseudohypoaldosteronism type 1
Synonyms:	autosomal dominant PHA 1, PHA1A
Definition:	A pseudohypoaldosteronism characterized by Salt wasting resulting from renal unresponsiveness to mineralocorticoids that has_material_basis_in heterozygous mutation in the NR3C2 gene on chromosome 4q31.
Ontology:	Human Disease [DOID:0060855]   ( DOID:0060855 )