creutzfeldt-jakob syndrome

Preferred Label : creutzfeldt-jakob syndrome;

MeSH definition : 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));

MeSH synonym : creutzfeldt jacob disease; jacob disease, creutzfeldt; cjd (creutzfeldt-jakob disease); jakob creutzfeldt syndrome; jakob-creutzfeldt syndrome; subacute spongiform encephalopathies; spongiform encephalopathies, subacute; disease, creutzfeldt-jakob; subacute spongiform encephalopathy; syndrome, jakob-creutzfeldt; spongiform encephalopathy, subacute; encephalopathies, subacute spongiform; encephalopathy, subacute spongiform; cjd (creutzfeldt jakob disease); creutzfeldt jakob disease; disease, creutzfeldt jacob; creutzfeldt-jakob disease; syndrome, creutzfeldt-jakob; jakob-creutzfeldt disease; disease, jakob-creutzfeldt; jakob creutzfeldt disease; creutzfeldt jakob syndrome;

CISMeF synonym : Creutzfeldt-Jakob; cjd variant (v-cjd); cjd; variant, cjd (v-cjd); variants, cjd (v-cjd); cjd variant (v cjd); cjd variants (v-cjd); cjds (creutzfeldt-jakob disease); Creutzfeldt Jakob; creutzfeldt-jakob's syndrome;

MeSH hyponym : new variant Creutzfeldt-Jakob disease; Creutzfeldt-Jakob disease, familial; Creutzfeldt Jakob Disease, Familial; Creutzfeldt-Jakob Diseases, Familial; Disease, Familial Creutzfeldt-Jakob; Familial Creutzfeldt-Jakob Diseases; Familial Creutzfeldt-Jakob Disease; Familial Creutzfeldt Jakob Disease; New Variant Creutzfeldt Jakob Disease; Creutzfeldt-Jakob Disease, Variant; Creutzfeldt Jakob Disease, Variant; Creutzfeldt-Jakob Disease, New Variant; Creutzfeldt Jakob Disease, New Variant; Variant Creutzfeldt-Jakob Disease; Variant Creutzfeldt Jakob Disease; V-CJD (Variant-Creutzfeldt-Jakob Disease); V CJD (Variant Creutzfeldt Jakob Disease);

Details

Origin ID

D007562;

UMLS CUI

C0022336;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- transmission [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
DO Cross reference
- Creutzfeldt-Jakob disease [DO Concept]
Manual NTBT mappings (CISMeF)
- Infectious disease with dementia [ORDO Disease]
MedlinePlus topic(s)
- creutzfeldt-jakob disease [MedlinePlus Topic]
ORDO relation(s)
- Sporadic Creutzfeldt-Jakob disease [ORDO Disease]
Record concept(s)
- Creutzfeldt-Jakob disease, familial [MeSH concept]
- Creutzfeldt-Jakob syndrome [MeSH concept]
- new variant Creutzfeldt-Jakob disease [MeSH concept]
Related MeSH Supplementary Concept(s)
- Creutzfeldt-Jakob disease, heidenhain variant [MeSH Supplementary Concept]
- Creutzfeldt-Jakob disease, sporadic [MeSH Supplementary Concept]
- acquired CJD [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- encephalopathy, bovine spongiform [MeSH Descriptor]
- kuru [MeSH Descriptor]
See also inter- (CISMeF)
- Variant Creutzfeldt-Jakob Disease [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CJ disease [MedDRA LLT]
- CJD [MedDRA LLT]
- CREUTZFELDT-JAKOB DISEASE [WHO-ART Preferred Term]
- Creutzfeld-Jacob disease [MedDRA LLT]
- Creutzfeld-Jakob disease [MedDRA LLT]
- Creutzfeldt-Jakob Disease [NCIt concept]
- Creutzfeldt-Jakob disease [MedDRA Preferred Term]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category (who)]
- Creutzfeldt-Jakob disease [DO Concept]
- Creutzfeldt-jakob disease [OMIM Phenotype]
- Genetic Creutzfeldt-Jakob disease [ICD-11 Subcategory]
- Jacob-Creutzfeld disease [MedDRA LLT]
- Jakob-Creutzfeldt disease [ICD-9 code]
- Jakob-Creutzfeldt disease [MedDRA LLT]
- Jakob-Creutzfeldt disease (disorder) [SNOMED CT concept]
- Sporadic Creutzfeldt-Jakob disease [ORDO Disease]
- creutzfeldt-jakob disease [MedlinePlus Topic]
- jakob-creutzfeldt disease [SNOMED Notion]
- transmissible virus dementia [SNOMED Notion]
Validated automatic mappings to BTNT
- familial Creutzfeldt Jakob disease [Disease (Nov.)]
- variant Creutzfeldt Jakob disease [Disease (Nov.)]

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