loading...| Preferred Name |
Creutzfeldt-Jakob disease |
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| Synonyms |
JAKOB CREUTZFELDT DIS |
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| Definitions |
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 promi (source : MSH) |
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| ID |
http://doe-generated-ontology.com/OntoAD#C0022336 |
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| altLabel |
JAKOB CREUTZFELDT DIS JCD Jakob-Creutzfeldt dis CJD (Creutzfeldt-Jakob Disease) Maladie de Jacob-Creutzfeld Maladie de Jakob-Creutzfeld Maladie de Creutzfeld-Jakob Creutzfeldt Jakob SPONGIFORM ENCEPH SUBACUTE JCD Jakob-Creutzfeldt disease Creutzfeldt-Jakob Syndrome CJD Creutzfeld-Jakob di Syndrome de Creutzfeldt-Jakob Pseudosclérose spastique de Jakob Maladie de Creutzfeld-Jacob CJD CREUTZFELDT JAKOB DIS Transmissible virus dementia Creutzfeldt-Jakob pseudosclerosis Pseudo-sclérose spastique de Jakob CJ disease MCJ Jakob-Creutzfeldt disease Creutzfeldt Jacob Disease Creutzfeldt-Jakob Creutzfeldt-Jakob Encéphalopathie spongiforme subaigüe Jacob-Creutzfeld disease Creutzfeld-Jakob disease Spongiform Encephalopathy, Subacute MCJ (Maladie de Creutzfeldt-Jakob) Maladie de CJ spastic; pseudosclerosis démence virale transmissible Encéphalopathie spongiforme subaiguë CJD maladie de Jakob-Creutzfeldt Creutzfeldt–Jakob |
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| clinically_similar | ||
| 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 promi (source : MSH) |
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| disease_has_associated_anatomic_site | ||
| disease_has_associated_gene | ||
| disease_has_primary_anatomic_site | ||
| has_associated_morphology | ||
| has_finding_site | ||
| has_manifestation |
http://doe-generated-ontology.com/OntoAD#C0003537 http://doe-generated-ontology.com/OntoAD#C0344315 http://doe-generated-ontology.com/OntoAD#C0009676 http://doe-generated-ontology.com/OntoAD#C0497327 http://doe-generated-ontology.com/OntoAD#C0240735 http://doe-generated-ontology.com/OntoAD#C0011253 http://doe-generated-ontology.com/OntoAD#C0751295 http://doe-generated-ontology.com/OntoAD#C0085632 http://doe-generated-ontology.com/OntoAD#C0027066 |
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| has_severity | ||
| hiddenLabel |
Creutzfeldt-JakobDisease MaladieDeCreutzfeldt-Jakob |
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| prefixIRI |
OntoAD:C0022336 |
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| prefLabel |
Maladie de Creutzfeldt-Jakob Creutzfeldt-Jakob disease |
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| subClassOf |