DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 17

Hereditary spastic paraplegia 17 [DOID:0110770]

A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12.

Synonyms:  hereditary spastic paraplegia 17,  DOID:0110770,  familial spastic paraplegia 17,  autosomal dominant spastic paraplegia 17,  autosomal dominant spastic paraplegia type 17 ...