Summary Literature (0)

DOID:0110811 - hereditary spastic paraplegia 6

Disease Ontology Definition: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: FSP3, SPG6, autosomal dominant familial spastic paraplegia type 3, autosomal dominant spastic paraplegia 6, autosomal dominant spastic paraplegia type 6,

Echinobase Genes :


OMIM:

MIM:600363 - spastic paraplegia 6, autosomal dominant; spg6

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee