An inherited blood disorder characterized by a decreased synthesis of one of the polypeptide chains that form hemoglobin. Anemia results from this abnormal hemoglobin formation. [ NCIT:P378 ]

Synonyms: α- and β-thalassemia sickle-cell thalassemia without crisis sickle-cell thalassemia with crisis thalassemia thalassemia Hb-S disease without crisis thalassemia Hb-S disease with crisis

This is just here as a test because I lose it

Term information

database cross reference
  • MONDO:0000984
  • ICD9:282.40 (DOID:10241)
  • NCIt:C35069
  • SCTID:40108008 (MONDO:equivalentTo)
  • ICD9:282.4 (i2s)
  • DOID:10241 (MONDO:equivalentTo)
  • GARD:0007756 (shared-xref)
  • ICD9:282.49 (i2s)
  • MeSH:D013789
  • ICD10:D56.9 (DOID:10241)
  • UMLS:C0039730 (NCIT:C35069)
  • ICD10:D56 (MONDO:equivalentTo)
  • MESH:D013789 (MONDO:equivalentTo)
  • COHD:30978 (MONDO:equivalentTo)
  • NCIT:C35069 (MONDO:equivalentTo)


excluded subClassOf



term editor

Gautier Koscielny

Term relations