congenital dyserythropoietic anemia type 2

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Disease Overview

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


Synonyms

  • CDA II
  • CDA type 2
  • CDA type II
  • CDAN2
  • Cda 2
  • SEC23B-CDG
  • anemia, congenital dyserythropoietic, type 2
  • anemia, congenital dyserythropoietic, type II
  • anemia, dyserythropoietic, congenital type 2
  • congenital dyserythropoietic anemia type 2
  • dyserythropoietic Anemia, congenital, type 2
  • dyserythropoietic Anemia, hempas type
  • dyserythropoietic anemia, congenital, type II
  • hempas anaemia
  • hempas anemia
  • hereditary erythroblastic multinuclearity with Positive acidified-serum test
  • hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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National Organization for Rare Disorders