JSON

familial hyperreninemic hypoaldosteronism type 1

^ http://purl.obolibrary.org/obo/MONDO_0020489

Term info

database cross reference
  • UMLS:C4289986 (MONDO:equivalentTo)
  • Orphanet:99763 (MONDO:equivalentTo)
Subsets

ordo_etiological_subtype

abbreviation
FHHA1 [ Orphanet:99763 ]

exactMatch

http://purl.obolibrary.org/obo/Orphanet_99763, http://linkedlifedata.com/resource/umls/id/C4289986

has exact synonym

18-hydroxylase deficiency, CMO I, 18-oxidase deficiency, FHHA1, corticosterone methyloxidase deficiency type I, CMO II, aldosterone synthase deficiency

id

MONDO:0020489

Term relations