hereditary thrombocytopenia and hematologic cancer predisposition syndrome

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Disease Overview

The disorder is characterized by thrombocytopenia of varying severity and a predisposition to hematologic malignancies. It may be caused due to germ line variations in the RUNX1, ETV6 or ANKRD26 genes.


Synonyms

  • familial platelet syndrome with predisposition to acute myelogenous leukaemia
  • familial thrombocytopenia with propensity to acute myelogenous leukaemia
  • hereditary thrombocytopenia and hematologic cancer predisposition syndrome
  • thrombocytopenia, familial, with propensity to acute myelogenous leukaemia

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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