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Disease Ontology Browser
hereditary spastic paraplegia 4 (DOID:0110792)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 4; autosomal dominant spastic paraplegia type 4; SPG4
Alt IDs: OMIM:182601, ICD10CM:G11.4, ORDO:100985
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.

Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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MGI 6.16
The Jackson Laboratory