Summary Literature (0)

DOID:0110791 - hereditary spastic paraplegia 3A

Disease Ontology Definition:A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22.

Synonyms: FSP1, SPG3A, autosomal dominant familial spastic paraplegia 1, autosomal dominant spastic paraplegia 3, autosomal dominant spastic paraplegia type 3, strumpell disease,

Echinobase Genes :


OMIM:

MIM:182600 - spastic paraplegia 3, autosomal dominant; spg3a

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

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