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Congenital dyserythropoietic anemia type II

^ http://www.orpha.net/ORDO/Orphanet_98873


Congenital dyserythropoietic anemia type II (CDA II) is the most common form of CDA (see this term) characterized by anemia, jaundice and splenomegaly and often leading to liver iron overload and gallstones.

Synonyms: CDA II, CDA type 2, Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas), Congenital dyserythropoietic anemia type 2, CDA type II, SEC23B-CDG

Term info

database cross reference
  • ICD-10:D64.4 (NTBT (narrower term maps to a broader term))
  • UMLS:C1306589 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:D64.4 (Attributed)
  • OMIM:224100 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

ICD-10:D64.4, OMIM:224100, UMLS:C1306589

notation

ORPHA:98873