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 ...