loading...| Preferred Name | hereditary spastic paraplegia | |
| Synonyms |
French settlement disease hereditary spastic paraparesis familial spastic paraplegia Strumpell-Lorrain disease |
|
| Definitions |
A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. Xref MGI. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_2476 |
|
| comment |
Xref MGI. |
|
| alternative label |
French settlement disease hereditary spastic paraparesis familial spastic paraplegia Strumpell-Lorrain disease |
|
| 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. Xref MGI. |
|
| has exact synonym |
French settlement disease hereditary spastic paraparesis familial spastic paraplegia Strumpell-Lorrain disease |
|
| has symptom | ||
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:2476 |
|
| in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus |
|
| label |
hereditary spastic paraplegia |
|
| notation |
DOID:2476 |
|
| note |
A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. Xref MGI. |
|
| preferred label |
hereditary spastic paraplegia |
|
| prefLabel |
hereditary spastic paraplegia |
|
| subClassOf |