hereditary spastic paraplegia 4

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

: spast

OMIM:

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

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

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

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

Parent(s): hereditary spastic paraplegia (is_a)