Sporadic Creutzfeldt-Jakob disease (sCJD) is a subacute fatal neurodegenerative disease belonging to the group of prion diseases, characterized by a clinical triad of dementia, myoclonus, and EEG anomalies, along with neuropathological evidence of neuronal loss, spongiform changes, and astrocytosis. There are three types of CJD: sporadicCJD (sCJD), inherited CJD, and iatrogenic and variant CJD (vCJD). [ Orphanet:204 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:204 (MONDO:equivalentTo)
  • SCTID:713060000 (MONDO:equivalentTo)
  • MedDRA:10011384 (Orphanet:204)
  • ICD10:A81.0 (Orphanet:204)
  • ICD9:046.19 (i2s)
Subsets

ordo_disease

definition

Sporadic Creutzfeldt-Jakob disease (sCJD) is a subacute fatal neurodegenerative disease belonging to the group of prion diseases, characterized by a clinical triad of dementia, myoclonus, and EEG anomalies, along with neuropathological evidence of neuronal loss, spongiform changes, and astrocytosis. There are three types of CJD: sporadicCJD (sCJD), inherited CJD, and iatrogenic and variant CJD (vCJD).

exactMatch

http://identifiers.org/snomedct/713060000

http://identifiers.org/meddra/10011384

http://www.orpha.net/ORDO/Orphanet_204

http://linkedlifedata.com/resource/umls/id/C0022336

has exact synonym

sporadic CJD

id

MONDO:0016079

Term relations