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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](img/icons/info1.png)
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