hereditary spastic paraplegia 41 (DOID:0110793)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 41; autosomal dominant spastic paraplegia type 41; SPG41
Alt IDs: OMIM:613364, ICD10CM:G11.4, ORDO:320355
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.