Tn polyagglutination syndrome (DOID:0080520)
Alliance: disease page
Synonyms: galactosyltransferase deficiency
Alt IDs: OMIM:300622
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.