DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 41

Hereditary spastic paraplegia 41 [DOID:0110793]

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.

Synonyms:  hereditary spastic paraplegia 41,  DOID:0110793,  familial spastic paraplegia 41,  SPG41,  autosomal dominant spastic paraplegia 41 ...