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inherited aplastic anemia

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes leukopenia and thrombocytopenia.

Synonyms

  • congenital aplastic anaemia
  • congenital aplastic anemia
  • congenital hypoplastic anaemia
  • congenital hypoplastic anemia
  • constitutional aplastic anaemia
  • constitutional aplastic anemia
  • hereditary aplastic anaemia
  • hereditary aplastic anemia
  • hypoplastic anaemia - familial
  • hypoplastic anemia - familial
  • rare constitutional aplastic anaemia
  • rare constitutional aplastic anemia
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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