Human genes for hereditary spastic paraplegia 42
Hereditary spastic paraplegia 42 [DOID:0110794]
A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.
Synonyms: hereditary spastic paraplegia 42, DOID:0110794, familial spastic paraplegia 42, autosomal dominant spastic paraplegia 42, autosomal dominant spastic paraplegia type 42 ...