Hereditary Spastic Paraplegia 3A
Disease ID: disease_node_16688
Connections displayed (default: 10).
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| Dbxref | GARD:5041, ICD10CM:G11.4, MIM:182600, ORDO:100984 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | FSP1, SPG3A, autosomal dominant familial spastic paraplegia 1, autosomal dominant spastic paraplegia 3, autosomal dominant spastic paraplegia type 3, strumpell disease |
| Doid Label | hereditary spastic paraplegia 3A |
| Doid Description | A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22. |
| Has Symptom | SYMP_0000094 |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16688 |
| Doid Id | DOID_0110791 |
| Label | Hereditary Spastic Paraplegia 3A |
- Outgoing r'ship
HAS_SYMPTOMto/from Muscle Weakness(ID:disease_node_9835;disease_node_21022) (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)