Hereditary Spastic Paraplegia 43
Disease ID: disease_node_16684
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G11.4, MIM:615043, ORDO:320370 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG43, autosomal recessive spastic paraplegia 43, autosomal recessive spastic paraplegia type 43 |
| Doid Label | hereditary spastic paraplegia 43 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16684 |
| Doid Id | DOID_0110795 |
| Label | Hereditary Spastic Paraplegia 43 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease)