JSON

inherited hemoglobinopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0019050

An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule. [ NCIT:C3092 ]

Synonyms: hemoglobinopathies Hemoglobinopathies / iron metabolism hereditary hemoglobinopathy

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:68364 (MONDO:equivalentTo)
  • MedDRA:10060892 (Orphanet:68364/e)
  • ICD10CM:D58.1 (Orphanet:68364/btnt)
  • SCTID:427306008 (MONDO:equivalentTo)
  • DOID:2860 (MONDO:equivalentTo)
  • NCIT:C3092 (MONDO:exact-label-match)
  • ICD9:282.7 (MONDO:relatedTo)
  • ICD10CM:D58.0 (Orphanet:68364/btnt)
  • MESH:D006453 (Orphanet:68364/e)
  • GARD:18883 (Orphanet:68364)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10060892

exactMatch

http://identifiers.org/snomedct/427306008

http://purl.obolibrary.org/obo/DOID_2860

http://identifiers.org/mesh/D006453

http://purl.obolibrary.org/obo/NCIT_C3092

http://www.orpha.net/ORDO/Orphanet_68364

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0003689

has related synonym

hemoglobinopathy

id

MONDO:0019050

Term relations