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Summary Literature (0)
DOID:0112125 - alpha-thalassemia myelodysplasia syndrome

Disease Ontology 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.

Synonyms: ATMDS, acquired HbH disease, acquired hemoglobin H disease, alpha-thalassemia-myelodysplastic syndrome,

Xenbase Genes : atrx



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): syndrome (is_a)