Hereditary Spastic Paraplegia 15
Disease ID: disease_node_16640
Connections displayed (default: 10).
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| Dbxref | GARD:9581, ICD10CM:G11.4, MIM:270700, ORDO:100996 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | Kjellin syndrome, SPG15, autosomal recessive spastic paraplegia 15, autosomal recessive spastic paraplegia type 15, hereditary spastic paraparesis type 15, spastic paraplegia and retinal degeneration, spastic paraplegia-retinal degeneration syndrome |
| Doid Label | hereditary spastic paraplegia 15 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16640 |
| Doid Id | DOID_0110768 |
| Label | Hereditary Spastic Paraplegia 15 |
- 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)