Search Ontology:
Human Disease

Tn polyagglutination syndrome

Term ID
DOID:0080520
Synonyms
  • galactosyltransferase deficiency
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. https://www.ncbi.nlm.nih.gov/pubmed/16251947
References
Ontology
Human Disease   ( DOID:0080520 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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