hereditary spastic paraplegia 45 (DOID:0110797)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 45; autosomal recessive spastic paraplegia type 45; autosomal recessive spastic paraplegia type 65; SPG45; SPG65
Alt IDs: OMIM:613162, ICD10CM:G11.4, ORDO:320396
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24.