Hereditary Spastic Paraplegia 35
Disease ID: disease_node_16693
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G11.4, MIM:612319, ORDO:171629 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | FAHN, SPG35, autosomal recessive spastic paraplegia 35, autosomal recessive spastic paraplegia type 35, fatty acid hydroxylase-associated neurodegeneration, leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia |
| Doid Label | hereditary spastic paraplegia 35 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16693 |
| Doid Id | DOID_0110786 |
| Label | Hereditary Spastic Paraplegia 35 |
- 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)