hereditary spastic paraplegia 61 (DOID:0110812)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 61; autosomal recessive spastic paraplegia type 61; SPG61
Alt IDs: OMIM:615685, ICD10CM:G11.4, ORDO:401780
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12.