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Disease Ontology Browser
hereditary spastic paraplegia (DOID:2476)
Alliance: disease page
Synonyms: familial spastic paraplegia; French settlement disease; hereditary spastic paraparesis; Strumpell-Lorrain disease
Alt IDs: ICD10CM:G11.4, ICD9CM:334.1, MESH:D015419, NCI:C140267, OMIM:PS303350, UMLS_CUI:C0037773
Definition: A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.

Disease References using Mouse Models (23)

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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last database update
MGI 6.13
The Jackson Laboratory