DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 13

Hereditary spastic paraplegia 13 [DOID:0110766]

A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 on chromosome 2q33.

Synonyms:  hereditary spastic paraplegia 13,  DOID:0110766,  familial spastic paraplegia 13,  autosomal dominant spastic paraplegia 13,  SPG13