OBO ID: DOID:0080520
Term Name: Tn polyagglutination syndrome Search Ontology:
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 Tn polyagglutination syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
C1GALT1C1 Tn polyagglutination syndrome, somatic 300622
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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