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Human Disease

alpha-thalassemia myelodysplasia syndrome

Term ID
DOID:0112125
Synonyms
  • acquired HbH disease
  • acquired hemoglobin H disease
  • alpha-thalassemia-myelodysplastic syndrome
  • ATMDS
Definition
A syndrome characterized by acquired alpha-thalassemia in association with a multilineage myelodysplasia that has_material_basis_in somatic mutation in the ATRX gene on chromosome Xq21.1. https://pubmed.ncbi.nlm.nih.gov/12858175/
References
Ontology
Human Disease   ( DOID:0112125 )
Relationships
is a type of
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Genes Involved
Zebrafish Models