OBO ID: DOID:2476
Term Name: hereditary spastic paraplegia Search Ontology:
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
  • NCI:C140267
  • OMIM:PS303350
  • SNOMEDCT_US_2020_09_01:267692008
  • UMLS_CUI:C0037773
Ontology: Human Disease   (DOID:2476)
Relationships
is a type of:
has subtype:
OTHER hereditary spastic paraplegia PAGES
GENES INVOLVED No data available
PHENOTYPE No data available

CITATIONS (7)