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hereditary spastic paraplegia 35
Summary
- Synonym
-
- FAHN
- SPG35
- autosomal recessive spastic paraplegia 35
- autosomal recessive spastic paraplegia type 35
- fatty acid hydroxylase-associated neurodegeneration
- leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.
- Super Class
- autosomal recessive disease hereditary spastic paraplegia
External Links
- Disease Ontology
- DOID:0110786
- Mondo Disease Ontology
- ORDO
- OMIM
- MGI genotype (from TogoID)
