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. |
|
| database_cross_reference |
NCI:C140267 UMLS_CUI:C0037773 ICD9CM:334.1 ICD10CM:G11.4 SNOMEDCT_US_2021_09_01:267692008 OMIM:PS303350 GARD:6637 MESH:D015419 |
|
| 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_obo_namespace |
disease_ontology |
|
| has_symptom | ||
| IAO_0000115 |
A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. |
|
| id |
DOID:2476 |
|
| in_subset | ||
| 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. |
|
| prefLabel |
hereditary spastic paraplegia |
|
| subClassOf |