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Summary Literature (0)
DOID:0110792 - hereditary spastic paraplegia 4

Disease Ontology Definition:A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22.

Synonyms: SPG4, autosomal dominant spastic paraplegia 4, autosomal dominant spastic paraplegia type 4,

Echinobase Genes : spast

MIM:182601 - spastic paraplegia 4, autosomal dominant; spg4

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spastic paraplegia (is_a)