Terminology Service for NFDI4Health
A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
Instance info
Synonyms
CJD (Creutzfeldt Jakob Disease), Jakob Creutzfeldt Disease, New Variant Creutzfeldt Jakob Disease, Variant Creutzfeldt-Jakob Disease, Spongiform Encephalopathies, Subacute, Spongiform Encephalopathy, Subacute, Creutzfeldt Jacob Disease, Disease, Creutzfeldt Jacob, Jakob-Creutzfeldt-Syndrom (DE), Familial Creutzfeldt-Jakob Disease, Creutzfeldt-Jakob-Syndrom (DE), Creutzfeldt-Jakob Disease, New Variant, Creutzfeldt-Jakob Diseases, Familial, V-CJD (Variant-Creutzfeldt-Jakob Disease), Syndrome, Creutzfeldt-Jakob, Creutzfeldt Jakob Disease, Variant, Syndrome, Jakob-Creutzfeldt, CJD (Creutzfeldt-Jakob Disease), Creutzfeldt-Jakob Disease, Familial, Variant Creutzfeldt Jakob Disease, Creutzfeldt Jakob Disease, New Variant, Encephalopathies, Subacute Spongiform, Disease, Jakob-Creutzfeldt, New Variant Creutzfeldt-Jakob Disease, Disease, Creutzfeldt-Jakob, V CJD (Variant Creutzfeldt Jakob Disease), Disease, Familial Creutzfeldt-Jakob, Jakob-Creutzfeldt Syndrome, Jakob Creutzfeldt Syndrome, Creutzfeldt Jakob Disease, Jacob Disease, Creutzfeldt, Creutzfeldt-Jakob Disease, Variant, Familial Creutzfeldt-Jakob Diseases, Creutzfeldt Jakob Disease, Familial, Creutzfeldt Jakob Syndrome, Encephalopathy, Subacute Spongiform, Subacute Spongiform Encephalopathies, Creutzfeldt-Jakob Disease, Spongiforme Enzephalopathie, subakute (DE), Neue Variante der Creutzfeld-Jakob-Krankheit (DE), Jakob-Creutzfeldt Disease, Enzephalopathie, subakute spongiöse (DE), Familial Creutzfeldt Jakob Disease, CJD-Variante (V-CJD) (DE), Subacute Spongiform Encephalopathy
AQL
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH TM UR VE VI
DC
1
DX
19730101
HN
1991; use JAKOB-CREUTZFELDT SYNDROME 1981-1990, use CREUTZFELDT-JAKOB DISEASE 1969-1980
MDA
19990101
MMR
20150603
MN
C10.228.228.800.230,C10.228.140.380.165,F03.615.400.300
PM
1991; see JAKOB-CREUTZFELDT SYNDROME 1981-1990, see CREUTZFELDT-JAKOB DISEASE 1973-1980
QB
http://purl.bioontology.org/ontology/MESH/Q000175,http://purl.bioontology.org/ontology/MESH/Q000097,http://purl.bioontology.org/ontology/MESH/Q000196,http://purl.bioontology.org/ontology/MESH/Q000151,http://purl.bioontology.org/ontology/MESH/Q000150,http://purl.bioontology.org/ontology/MESH/Q000191,http://purl.bioontology.org/ontology/MESH/Q000139,http://purl.bioontology.org/ontology/MESH/Q000534,http://purl.bioontology.org/ontology/MESH/Q000235,http://purl.bioontology.org/ontology/MESH/Q000532,http://purl.bioontology.org/ontology/MESH/Q000378,http://purl.bioontology.org/ontology/MESH/Q000652,http://purl.bioontology.org/ontology/MESH/Q000134,http://purl.bioontology.org/ontology/MESH/Q000453,http://purl.bioontology.org/ontology/MESH/Q000178,http://purl.bioontology.org/ontology/MESH/Q000276,http://purl.bioontology.org/ontology/MESH/Q000451,http://purl.bioontology.org/ontology/MESH/Q000473,http://purl.bioontology.org/ontology/MESH/Q000000981,http://purl.bioontology.org/ontology/MESH/Q000517,http://purl.bioontology.org/ontology/MESH/Q000635,http://purl.bioontology.org/ontology/MESH/Q000382,http://purl.bioontology.org/ontology/MESH/Q000469,http://purl.bioontology.org/ontology/MESH/Q000821,http://purl.bioontology.org/ontology/MESH/Q000601,http://purl.bioontology.org/ontology/MESH/Q000523,http://purl.bioontology.org/ontology/MESH/Q000401,http://purl.bioontology.org/ontology/MESH/Q000201,http://purl.bioontology.org/ontology/MESH/Q000662,http://purl.bioontology.org/ontology/MESH/Q000266,http://purl.bioontology.org/ontology/MESH/Q000145,http://purl.bioontology.org/ontology/MESH/Q000188,http://purl.bioontology.org/ontology/MESH/Q000628,http://purl.bioontology.org/ontology/MESH/Q000209,http://purl.bioontology.org/ontology/MESH/Q000208,http://purl.bioontology.org/ontology/MESH/Q000503
SIB
http://purl.bioontology.org/ontology/MESH/D057174,http://purl.bioontology.org/ontology/MESH/D018888,http://purl.bioontology.org/ontology/MESH/D016643,http://purl.bioontology.org/ontology/MESH/D015526,http://purl.bioontology.org/ontology/MESH/D006816,http://purl.bioontology.org/ontology/MESH/D007729,http://purl.bioontology.org/ontology/MESH/D055956,http://purl.bioontology.org/ontology/MESH/D020232,http://purl.bioontology.org/ontology/MESH/D012608,http://purl.bioontology.org/ontology/MESH/D034081,http://purl.bioontology.org/ontology/MESH/D015140,http://purl.bioontology.org/ontology/MESH/D016098,http://purl.bioontology.org/ontology/MESH/D020961,http://purl.bioontology.org/ontology/MESH/D034062,http://purl.bioontology.org/ontology/MESH/D000544
TERMUI
T022729,T022734,T367205,T367204,T367210,T022730,T022731,T022732,T812338,T752045,T752046,T367207,T367209,T367208
TH
NLM (1991),NLM (1969),ORD (2010),OMIM (2013),NLM (2000),NLM (2010),UNK (19XX),NLM (1997)
cui
C0376329,C0022336,C0751254
hasSTY
http://purl.bioontology.org/ontology/STY/T047
mapped from
http://purl.bioontology.org/ontology/MESH/C565143,http://purl.bioontology.org/ontology/MESH/C566981,http://purl.bioontology.org/ontology/MESH/C538481
tui
T047
Instance relations
Types