FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term alpha-thalassemia myelodysplasia syndrome ID (Ontology) DOID:0112125 (Human Disease)
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.
Also Known As "acquired HbH disease" ; "acquired hemoglobin H disease" ; "alpha-thalassemia-myelodysplastic syndrome" (for all, see Synonyms field below)
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 Genes
 alpha-thalassemia myelodysplasia syndrome       2
 for disease ribbon | alpha-thalassemia myelodysplasia syndrome       2
 model of | alpha-thalassemia myelodysplasia syndrome       2
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       |__alpha-thalassemia myelodysplasia syndrome  2 rec.
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Synonyms
  • "acquired HbH disease" EXACT
    "acquired hemoglobin H disease" EXACT
    "alpha-thalassemia-myelodysplastic syndrome" EXACT
    "ATMDS" EXACT OMO:0003012
Secondary IDs
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MESH:C563023
MIM:300448
ORDO:231401
SNOMEDCT_US_2023_03_01:307343001
UMLS_CUI:C0585216