A progressive autoimmune disorder affecting the central nervous system resulting in demyelination. Patients develop physical and cognitive impairments that correspond with the affected nerve fibers. [ NCIT : P378 ]
This is just here as a test because I lose it
Term information
database
cross reference
- Orphanet:802 (MONDO:equivalentTo)
- ICD9:340 (EFO:0003885)
- EFO:0003885 (MONDO:equivalentTo)
- MESH:D009103 (MONDO:equivalentTo)
- DOID:2377 (MONDO:equivalentTo)
- UMLS:C0026769 (NCIT:C3243)
- ICD10CM:G35 (MONDO:equivalentTo)
- SCTID:24700007 (MONDO:equivalentTo)
- NCIT:C3243 (MONDO:equivalentTo)
exactMatch
- http://purl.obolibrary.org/obo/Orphanet_802
- http://purl.bioontology.org/ontology/ICD10CM/G35
- http://identifiers.org/snomedct/24700007
- http://linkedlifedata.com/resource/umls/id/C0026769
- http://purl.obolibrary.org/obo/DOID_2377
- http://identifiers.org/mesh/D009103
- http://purl.obolibrary.org/obo/NCIT_C3243
gwas trait
- true
has narrow synonym
- generalized multiple sclerosis
has related synonym
- insular sclerosis
id
- MONDO:0005301