Search Ontology:
Human Disease
hereditary spastic paraplegia
- Term ID
- DOID:2476
- Synonyms
-
- familial spastic paraplegia
- French settlement disease
- hereditary spastic paraparesis
- Strumpell-Lorrain disease
- Definition
- A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. http://en.wikipedia.org/wiki/Familial_spastic_paraplegia
- References
-
- GARD:6637
- ICD10CM:G11.4
- ICD9CM:334.1
- MESH:D015419
- MIM:PS303350
- NCI:C140267
- SNOMEDCT_US_2023_03_01:267692008
- UMLS_CUI:C0037773
- Ontology
- Human Disease ( DOID:2476 )
- is a type of
-
- has subtype
Other Pages
Genes Involved
Zebrafish Models