hereditary spastic paraplegia 6 (DOID:0110811)
Alliance: disease page
Synonyms: autosomal dominant familial spastic paraplegia type 3; autosomal dominant spastic paraplegia 6; autosomal dominant spastic paraplegia type 6; FSP3; SPG6
Alt IDs: OMIM:600363, ICD10CM:G11.4, ORDO:100988
Definition: A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2.