hereditary spastic paraplegia 35
A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
hereditary spastic paraplegia 35
- 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
disease_ontology
DOID:0110786