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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: acquired HbH disease, acquired hemoglobin H disease, alpha-thalassemia-myelodysplastic syndrome, ATMDS
Xenbase Genes
:
atrx
| MIM:300448 - ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME; ATMDS |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)