hereditary spastic paraplegia
(Q657516)
genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs
genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs
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Current Data About
hereditary spastic paraplegia
(P31) |
(Q929833)
(Q112193867) |
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(P138) |
(Q65698)
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(P279) |
(Q1049655)
(Q19001236)
(Q12136) |
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(P373) |
Hereditary spastic paraplegia
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(P780) |
(Q1049655)
(Q117060)
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(P1692) |
334.1
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(P1748) |
C140267
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(P1995) |
(Q83042)
|
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(P2293) |
(Q14865255)
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(P2888) |
http://purl.obolibrary.org/obo/DOID_2476
http://identifiers.org/doid/DOID:2476
http://www.orpha.net/ORDO/Orphanet_685 |
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(P5008) |
(Q4099686)
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other details
aliases |
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 |
description | genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs |
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