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DOID:0060855 - autosomal dominant pseudohypoaldosteronism type 1
Disease Ontology 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.
Synonyms: PHA1A, autosomal dominant PHA 1,
Echinobase Genes :
MIM:177735 - pseudohypoaldosteronism, type i, autosomal dominant; pha1a |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee