hereditary spastic paraplegia 43
Information
- Disease name
- hereditary spastic paraplegia 43
- Disease ID
- DOID:0110795
- Description
- "A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12." [url:https\://www.ncbi.nlm.nih.gov/pubmed/23857908]
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)
- ICD10CM:G11.4
- Cross Reference ID (Disease Ontology)
- MIM:615043
- Cross Reference ID (Disease Ontology)
- ORDO:320370
- Exact Synonym (Disease Ontology)
- autosomal recessive spastic paraplegia 43
- Exact Synonym (Disease Ontology)
- autosomal recessive spastic paraplegia type 43
- Exact Synonym (Disease Ontology)
- SPG43