DISEASES

Disease-gene associations mined from literature

Human genes for hereditary spastic paraplegia 38

Hereditary spastic paraplegia 38 [DOID:0110789]

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15.

Synonyms:  hereditary spastic paraplegia 38,  DOID:0110789,  familial spastic paraplegia 38,  autosomal dominant spastic paraplegia 38,  autosomal dominant spastic paraplegia type 38 ...