Hereditary Spastic Paraplegia 4
Disease ID: disease_node_16687
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G11.4, MIM:182601, ORDO:100985 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG4, autosomal dominant spastic paraplegia 4, autosomal dominant spastic paraplegia type 4 |
| Doid Label | hereditary spastic paraplegia 4 |
| Doid Description | A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22. |
| Has Symptom | SYMP_0000363, SYMP_0000094 |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16687 |
| Doid Id | DOID_0110792 |
| Label | Hereditary Spastic Paraplegia 4 |
- Outgoing r'ship
HAS_SYMPTOMto/from Muscle Weakness(ID:disease_node_9835;disease_node_21022) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Progressive Weakness(ID:disease_node_21078) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)