hereditary spastic paraplegia English (Q657516)

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genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs English
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Language Label Description Also known as
English
hereditary spastic paraplegia
genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs
  • HSMN V
  • familial spastic paraplegia
  • Strümpell-Lorrain disease
  • French settlement disease
  • Strumpell-Lorrain disease
  • hereditary spastic paraparesis
  • FSP
  • HSP
  • SPG
  • StrC<mpell-Lorrain disease
  • Familial spastic paraparesis

Statements

instance of English
rare disease English
0 references
0 references
subclass of English
paraplegia English
1 reference
stated in English
retrieved English
30 November 2020
disease English
0 references
named after English
0 references
neurology English
0 references
paraplegia English
1 reference
stated in English
retrieved English
30 November 2020
spasticity English
1 reference
stated in English
retrieved English
30 November 2020
ICD-9-CM English
334.1
2 references
stated in English
retrieved English
15 May 2019
C140267
1 reference
Hereditary spastic paraplegia
0 references

Identifiers

Spastic Paraplegia, Hereditary
1 reference
stated in English
retrieved English
15 May 2019
0 references
0 references
0 references
0 references
KEGG ID English
0 references
1 reference
stated in English
retrieved English
30 November 2020
DiseasesDB English
eMedicine ID English
Freebase ID English
1 reference
stated in English
28 October 2013
2 references
stated in English
retrieved English
15 May 2019
ICD-10-CM English
2 references
stated in English
retrieved English
15 May 2019
0 references
8B44.0
Hereditary spastic paraplegia
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Mondo ID English
0 references
Orphanet ID English
1 reference
Hereditary spastic paraplegia
0 references
UMLS CUI English
1 reference
1 reference
stated in English
retrieved English
15 May 2019