Term info
- GARD:0006637 (MONDO:equivalentTo)
- OMIMPS:303350 (MONDO:equivalentTo)
- DOID:2476 (MONDO:equivalentTo)
- MedDRA:10019903 (Orphanet:685/e)
- ICD9:334.1 (MONDO:i2s)
- Orphanet:685 (MONDO:equivalentTo)
- NCIT:C140267 (MONDO:equivalentTo)
- SCTID:39912006 (MONDO:equivalentTo)
- ICD10CM:G11.4 (Orphanet:685/specific)
- MESH:D015419 (MONDO:equivalentTo)
gard_rare, disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10019903
Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.
http://purl.bioontology.org/ontology/ICD10CM/G11.4, https://omim.org/phenotypicSeries/PS303350, http://purl.obolibrary.org/obo/Orphanet_685, http://purl.obolibrary.org/obo/DOID_2476, http://purl.obolibrary.org/obo/NCIT_C140267, http://identifiers.org/mesh/D015419, http://identifiers.org/snomedct/39912006
spastic paraplegia
French settlement disease, HSP, Strümpell-Lorrain disease, familial spastic paraplegia, Strumpell-Lorrain disease, hereditary spastic paraparesis, SPG
FSP, familial spastic paraparesis
MONDO:0019064
https://rarediseases.info.nih.gov/diseases/6637/hereditary-spastic-paraplegia