hereditary spastic paraplegia 64 (DOID:0110815)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 64; autosomal recessive spastic paraplegia type 64; SPG64
Alt IDs: OMIM:615683, ICD10CM:G11.4, ORDO:401810
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24.