hereditary spastic paraplegia 30 (DOID:0110781)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 30; autosomal recessive spastic paraplegia 30; autosomal spastic paraplegia type 30; SPG30
Alt IDs: OMIM:610357, ICD10CM:G11.4, ORDO:101010
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37.