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autosomal dominant pseudohypoaldosteronism type 1

Go to external page http://purl.obolibrary.org/obo/MONDO_0008329

Renal pseudohypoaldosteronism type 1 (renal PHA1) is a mild form of primary mineralocorticoid resistance restricted to the kidney. [ Orphanet:171871 ]

Synonyms: PHA1A autosomal dominant PHA 1 pseudohypoaldosteronism type i, autosomal dominant autosomal dominant pseudohypoaldosteronism type 1

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:171871 (OMIM:177735)
  • NCIT:C126810 (MONDO:equivalentTo)
  • UMLS:C1449842 (Orphanet:171871)
  • OMIM:177735 (Orphanet:171871/e)
  • DOID:0060855 (MONDO:equivalentTo)
  • GARD:9145 (Orphanet:171871)
Subsets

gard_rare, ordo_clinical_subtype, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4521

exactMatch

https://omim.org/entry/177735

http://www.orpha.net/ORDO/Orphanet_171871

http://purl.obolibrary.org/obo/DOID_0060855

http://linkedlifedata.com/resource/umls/id/C1449842

http://purl.obolibrary.org/obo/NCIT_C126810

has related synonym

pseudohypoaldosteronism, type I, autosomal dominant

pseudohypoaldosteronism type 1, dominant

renal pseudohypoaldosteronism type 1

renal PHA1

PHA I, autosomal dominant

pseudohypoaldosteronism type 1 autosomal dominant

id

MONDO:0008329

seeAlso

https://rarediseases.info.nih.gov/diseases/9145/autosomal-dominant-pseudohypoaldosteronism-type-1

https://search.clinicalgenome.org/kb/conditions/MONDO:0008329

Term relations