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Hereditary spastic paraplegia

^ http://www.orpha.net/ORDO/Orphanet_685


Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.

Synonyms: HSP, Familial spastic paraplegia, Strümpell-Lorrain disease, Hereditary spastic paraparesis, SPG

Term info

database cross reference
  • UMLS:C0037773 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:G11.4 (Specific code (The term has its own code in the ICD10))
  • ICD-10:G11.4 (E (exact mapping (the terms and the concepts are equivalent)))
  • MedDRA:10019903 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C2931355 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

UMLS:C2931355, MedDRA:10019903, UMLS:C0037773, ICD-10:G11.4

notation

ORPHA:685

Term relations

Subclass of: