FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Tn polyagglutination syndrome ID (Ontology) DOID:0080520 (Human Disease)
Definition A hematopoietic system disease that is characterized by red blood cells that agglutinate upon exposure to almost all human sera, but not to autologous serum or the sera of newborns and has_material_basis_in somatic mutation in the C1GALT1C1 gene on chromosome Xq24.
Also Known As "galactosyltransferase deficiency"
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 Tn polyagglutination syndrome       3
 for disease ribbon | Tn polyagglutination syndrome       3
 model of | Tn polyagglutination syndrome       3
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   |__hematopoietic system disease
       |__Tn polyagglutination syndrome  3 rec.
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Is a hematopoietic system disease
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Synonyms
  • "galactosyltransferase deficiency" EXACT
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MIM:300622