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autosomal dominant pseudohypoaldosteronism type 1

Disease Summary
Associated Targets (12)
Tbio

7

Tclin

4

Tchem

1


GARD Rare
Mondo Description Renal pseudohypoaldosteronism type 1 (renal PHA1) is a mild form of primary mineralocorticoid resistance restricted to the kidney.
Uniprot Description A salt wasting disease resulting from target organ unresponsiveness to mineralocorticoids. PHA1A is a mild form characterized by target organ defects confined to kidney. Patients may present with neonatal renal salt wasting with hyperkalaemic acidosis despite high aldosterone levels. These patients improve with age and usually become asymptomatic without treatment.
Disease Ontology Description 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.
Mondo Term and Equivalent IDs
MONDO:0008329:  autosomal dominant pseudohypoaldosteronism type 1
GARD:0009145: 
NCIT:C126810: 
Orphanet:171871: 
UMLS:C1449842: