Tn Polyagglutination Syndrome
Disease ID: disease_node_17067
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| Dbxref | MIM:300622 |
|---|---|
| Subclassof | DOID_74 |
| Data Source | DOID |
| Synonyms | galactosyltransferase deficiency |
| Doid Label | Tn polyagglutination syndrome |
| Doid Description | 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. |
| Disease Node Id | disease_node_17067 |
| Doid Id | DOID_0080520 |
| Label | Tn Polyagglutination Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Hematologic Diseases(ID:disease_node_3773) (Disease)