hereditary spastic paraplegia 8
Information
- Disease name
- hereditary spastic paraplegia 8
- Disease ID
- DOID:0110823
- Description
- "A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24." [url:https\://www.ncbi.nlm.nih.gov/pubmed/17160902]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:2476
- Cross Reference ID (Disease Ontology)
- GARD:9591
- Cross Reference ID (Disease Ontology)
- ICD10CM:G11.4
- Cross Reference ID (Disease Ontology)
- MIM:603563
- Cross Reference ID (Disease Ontology)
- ORDO:100989
- Exact Synonym (Disease Ontology)
- autosomal dominant spastic paraplegia 8
- Exact Synonym (Disease Ontology)
- autosomal dominant spastic paraplegia type 8
- Exact Synonym (Disease Ontology)
- SPG8