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autosomal dominant pseudohypoaldosteronism type 1 (DOID:0060855)
Alliance: disease page
Synonyms: autosomal dominant PHA 1; PHA1A
Alt IDs: OMIM:177735, 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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory