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Human Disease
hereditary spastic paraplegia 35
- Term ID
- DOID:0110786
- Synonyms
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- autosomal recessive spastic paraplegia 35
- autosomal recessive spastic paraplegia type 35
- FAHN
- fatty acid hydroxylase-associated neurodegeneration
- leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
- SPG35
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. https://www.ncbi.nlm.nih.gov/pubmed/19068277
- References
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- ICD10CM:G11.4
- MIM:612319
- ORDO:171629
- Ontology
- Human Disease ( DOID:0110786 )
- is a type of
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Genes Involved
Zebrafish Models