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Creutzfeldt Jacob disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0005357

A rare transmittable degenerative disorder of the brain caused by prions. Morphologically it is characterized by spongiform degeneration of the cerebral and cerebellar cortex. Signs and symptoms include sleep disturbances, personality changes, aphasia, ataxia, muscle atrophy and weakness, visual loss, and myoclonus. It usually leads to death within a year from the onset of the disease. [ NCIT:P378 ]

Synonyms: Jakob-Creutzfeldt disease transmissible virus dementia CJD (Creutzfeldt Jakob disease) Creutzfeldt-Jacob disease Creutzfeldt Jakob Disease Subacute spongiform encephalopathy classic Creutzfeldt-Jakob disease CJD Creutzfeldt Jacob syndrome Creutzfeldt Jakob disease

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:046.19 (MONDO:relatedTo)
  • MESH:D007562 (MONDO:equivalentTo)
  • UMLS:C0022336 (MONDO:equivalentTo)
  • MEDGEN:7179 (MONDO:equivalentTo)
  • NORD:1014 (MONDO:NORD)
  • EFO:0004226 (MONDO:equivalentTo)
  • DOID:11949 (MONDO:equivalentTo)
  • SCTID:792004 (MONDO:equivalentTo)
  • NCIT:C26802 (MONDO:equivalentTo)
  • ICD9:046.1 (MONDO:i2s)
Subsets

gard_rare, otar, rare, nord_rare

abbreviation
CJD [ DOID:11949 ]

exactMatch

http://identifiers.org/snomedct/792004

http://purl.obolibrary.org/obo/DOID_11949

http://identifiers.org/medgen/7179

http://purl.obolibrary.org/obo/NCIT_C26802

http://identifiers.org/mesh/D007562

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

has related synonym

Creutzfeldt-Jakob disease

id

MONDO:0005357

Term relations

Subclass of: