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Alpha-thalassemia

^ http://www.orpha.net/ORDO/Orphanet_846


Alpha-thalassemia is an inherited hemoglobinopathy characterized by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles.

Term info

database cross reference
  • MedDRA:10043390 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C0002312 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C1456873 (E (exact mapping (the terms and the concepts are equivalent)))
  • MeSH:D017085 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:D56.0 (Specific code (The term has its own code in the ICD10))
  • ICD-10:D56.0 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:604131 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

MedDRA:10043390, MeSH:D017085, OMIM:604131, ICD-10:D56.0, UMLS:C1456873, UMLS:C0002312

notation

ORPHA:846