familial hyperreninemic hypoaldosteronism type 1

Go to external page http://purl.obolibrary.org/obo/MONDO_0020489


This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C4289986 (MONDO:equivalentTo)
  • ICD10:E27.4 (Orphanet:99763)
  • Orphanet:99763 (MONDO:equivalentTo)
Subsets

ordo_etiological_subtype

abbreviation
FHHA1 [ Orphanet:99763 ]

closeMatch

http://linkedlifedata.com/resource/umls/id/C0268293

exactMatch

http://www.orpha.net/ORDO/Orphanet_99763

http://linkedlifedata.com/resource/umls/id/C4289986

has exact synonym

18-hydroxylase deficiency

FHHA1

CMO I

18-oxidase deficiency

corticosterone methyloxidase deficiency type I

aldosterone synthase deficiency

CMO II

id

MONDO:0020489

Term relations