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Disease Ontology Browser
alpha-thalassemia myelodysplasia syndrome (DOID:0112125)
Alliance: disease page
Synonyms: acquired HbH disease; acquired hemoglobin H disease; alpha-thalassemia-myelodysplastic syndrome; ATMDS
Alt IDs: OMIM:300448, MESH:C563023, ORDO:231401, UMLS_CUI:C0585216
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory