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autosomal dominant pseudohypoaldosteronism type 1 (DOID:0060855)
Synonyms: autosomal dominant PHA 1; PHA1A
Alt IDs: OMIM:177735, ICD10CM:N25.8, MESH:D011546, ORDO:756, UMLS_CUI:C1449843
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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory