This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:E85.0 (Orphanet:93562)
  • Orphanet:93562 (MONDO:equivalentTo)
  • UMLS:CN206640 (MONDO:equivalentTo)
Subsets

ordo_clinical_subtype

exactMatch

http://www.orpha.net/ORDO/Orphanet_93562

http://linkedlifedata.com/resource/umls/id/CN206640

has exact synonym

hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant

fibrinogen A alpha-chain amyloidosis

familial amyloid nephropathy due to fibrinogen A alpha-chain variant

hereditary renal amyloidosis due to fibrinogen A alpha-chain variant

id

MONDO:0019733

Term relations