Galactosialidosis
Disease ID: disease_node_20486
Connections displayed (default: 10).
Loading graph...
| Dbxref | GARD:3953, MIM:256540 |
|---|---|
| Subclassof | DOID_3211 |
| Data Source | DOID |
| Doid Label | galactosialidosis |
| Doid Description | A lysosomal storage disease that is characterized by combined deficiency of beta-galactosidase and neuraminidase that has_material_basis_in homozygous or compound heterozygous mutation in the CTSA gene on chromosome 20q13. |
| Disease Node Id | disease_node_20486 |
| Doid Id | DOID_0080540 |
| Label | Galactosialidosis |
- Outgoing r'ship
SUBCLASS_OFto/from Lysosomal Storage Diseases(ID:disease_node_8717) (Disease)