DISEASES

Disease-gene associations mined from literature

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 ...