Hereditary Spastic Paraplegia 11
Disease ID: disease_node_16644
Connections displayed (default: 10).
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| Dbxref | GARD:4919, ICD10CM:G11.4, MIM:604360, ORDO:2822 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | HSP-TCC, Nakamura-Osame syndrome, SPG11, autosomal recessive spastic paraplegia 11, autosomal recessive spastic paraplegia complicated with thin corpus callosum, autosomal recessive spastic paraplegia type 11, autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum, spastic paraplegia-intellectual disability-thin corpus callosum syndrome |
| Doid Label | hereditary spastic paraplegia 11 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16644 |
| Doid Id | DOID_0110764 |
| Label | Hereditary Spastic Paraplegia 11 |
- 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)