hereditary spastic paraplegia 4

Summary

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,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: spast

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008438 - hereditary spastic paraplegia 4

MONDO:0008438 - hereditary spastic paraplegia 4

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

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

Parent(s): autosomal dominant disease (is_a), hereditary spastic paraplegia (is_a)