hereditary spastic paraplegia 15 (DOID:0110768)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 15; autosomal recessive spastic paraplegia type 15; hereditary spastic paraparesis type 15; Kjellin syndrome; spastic paraplegia and retinal degeneration; spastic paraplegia-retinal degeneration syndrome; SPG15
Alt IDs: OMIM:270700, ICD10CM:G11.4, ORDO:100996
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1.