# autosomal dominant pseudohypoaldosteronism type 1

> 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

**Wikidata**: [Q32136465](https://www.wikidata.org/wiki/Q32136465)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-pseudohypoaldosteronism-type-1


## References

1. Disease Ontology
2. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
3. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000151623/Orphanet_171871)
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. UMLS 2023