Human genes for hereditary spastic paraplegia 6
Hereditary spastic paraplegia 6 [DOID:0110811]
A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2.
Synonyms: hereditary spastic paraplegia 6, DOID:0110811, familial spastic paraplegia 6, autosomal dominant familial spastic paraplegia type 3, autosomal dominant spastic paraplegia 6 ...