Hereditary Spastic Paraplegia 88
Disease ID: disease_node_16676
Connections displayed (default: 10).
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| Dbxref | MIM:620106 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG88, autosomal dominant spastic paraplegia 88 |
| Doid Label | hereditary spastic paraplegia 88 |
| Doid Description | A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that slowly progresses with variable severity that has_material_basis_in heterozygous mutation in the KPNA3 gene on chromosome 13q14.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16676 |
| Doid Id | DOID_0070457 |
| Label | Hereditary Spastic Paraplegia 88 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease)