loading...| Preferred Name | hereditary spastic paraplegia | |
| Synonyms |
familial spastic paraparesis FSP spastic paraplegia familial spastic paraplegia Strümpell-Lorrain disease SPG hereditary spastic paraparesis HSP Strumpell-Lorrain disease French settlement disease |
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| Definitions |
Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0019064 |
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| altLabel |
familial spastic paraparesis FSP spastic paraplegia familial spastic paraplegia Strümpell-Lorrain disease SPG hereditary spastic paraparesis HSP Strumpell-Lorrain disease French settlement disease |
|
| definition |
Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs. |
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| has_broad_synonym |
spastic paraplegia |
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| has_exact_synonym |
familial spastic paraplegia Strümpell-Lorrain disease SPG hereditary spastic paraparesis HSP Strumpell-Lorrain disease French settlement disease |
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| has_related_synonym |
familial spastic paraparesis FSP |
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| label |
hereditary spastic paraplegia |
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| prefixIRI |
MONDO:0019064 |
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| prefLabel |
hereditary spastic paraplegia |
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| seeAlso |
https://rarediseases.info.nih.gov/diseases/6637/hereditary-spastic-paraplegia |
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| textual definition |
Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs. |
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| subClassOf |