hereditary spastic paraplegia 35
Information
- Disease name
- hereditary spastic paraplegia 35
- Disease ID
- DOID:0110786
- Description
- "A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1." [url:https\://www.ncbi.nlm.nih.gov/pubmed/19068277]
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:612319
- Cross Reference ID (Disease Ontology)
- ORDO:171629
- Exact Synonym (Disease Ontology)
- autosomal recessive spastic paraplegia 35
- Exact Synonym (Disease Ontology)
- autosomal recessive spastic paraplegia type 35
- Exact Synonym (Disease Ontology)
- FAHN
- Exact Synonym (Disease Ontology)
- fatty acid hydroxylase-associated neurodegeneration
- Exact Synonym (Disease Ontology)
- leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
- Exact Synonym (Disease Ontology)
- SPG35