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loading...| Preferred Name | hereditary spastic paraplegia | |
| Synonyms |
French settlement disease hereditary spastic paraparesis familial spastic paraplegia Strumpell-Lorrain disease |
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| Definitions |
A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. Xref MGI. |
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| ID |
http://purl.obolibrary.org/obo/DOID_2476 |
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| comment |
Xref MGI. |
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| database_cross_reference |
MIM:PS303350 UMLS_CUI:C0037773 ICD9CM:334.1 MESH:D015419 SNOMEDCT_US_2023_03_01:267692008 NCI:C140267 ICD10CM:G11.4 GARD:6637 |
|
| definition |
A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. |
|
| has exact synonym |
French settlement disease hereditary spastic paraparesis familial spastic paraplegia Strumpell-Lorrain disease |
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| has symptom | ||
| has_obo_namespace |
disease_ontology |
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| id |
DOID:2476 |
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| in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus |
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| label |
hereditary spastic paraplegia |
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| notation |
DOID:2476 |
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| prefLabel |
hereditary spastic paraplegia |
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| subClassOf |
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