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Congenital dyserythropoietic anemia type I

^ http://www.orpha.net/ORDO/Orphanet_98869


Congenital dyserythropoietic anemiatype I (CDA I) is a hematologic disorder of erythropoiesis characterized by moderate to severe macrocytic anemia occasionally associated with limb or nail deformities and scoliosis.

Synonyms: CDA type 1, CDA I, CDA type I, Congenital dyserythropoietic anemia type 1

Term info

database cross reference
  • UMLS:C0271933 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:615631 (BTNT (broader term maps to a narrower term))
  • ICD-10:D64.4 (Attributed)
  • ICD-10:D64.4 (NTBT (narrower term maps to a broader term))
  • OMIM:224120 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

OMIM:615631, ICD-10:D64.4, UMLS:C0271933, OMIM:224120

notation

ORPHA:98869