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 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models