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 |
|
| 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. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0019064 |
|
| closeMatch | ||
| database_cross_reference |
MedDRA:10019903 ICD9:334.1 ICD10:G11.4 NCIT:C140267 COHD:192901 SCTID:39912006 OMIMPS:303350 GARD:0006637 Orphanet:685 DOID:2476 MESH:D015419 |
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| disease has feature | ||
| exactMatch |
http://identifiers.org/snomedct/39912006 http://identifiers.org/mesh/D015419 http://linkedlifedata.com/resource/umls/id/C0037773 http://purl.obolibrary.org/obo/DOID_2476 http://identifiers.org/meddra/10019903 |
|
| has broad synonym |
spastic paraplegia |
|
| has exact synonym |
familial spastic paraplegia Strümpell-Lorrain disease SPG hereditary spastic paraparesis HSP Strumpell-Lorrain disease French settlement disease |
|
| has related synonym |
familial spastic paraparesis FSP |
|
| id |
MONDO:0019064 |
|
| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#gard_rare http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
hereditary spastic paraplegia |
|
| notation |
MONDO:0019064 |
|
| prefLabel |
hereditary spastic paraplegia |
|
| see also |
https://rarediseases.info.nih.gov/diseases/6637/hereditary-spastic-paraplegia |
|
| should_conform_to |
http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml |
|
| 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. |
|
| subClassOf |