Autosomal dominant hereditary disorder
Creutzfeldt-Jakob disease
Hereditary degenerative disease of central nervous system
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Familial Creutzfeldt-Jakob (disorder)
Familial Creutzfeldt-Jakob
Inherited Creutzfeldt-Jakob disease
fCJD (Familial Creutzfeldt-Jakob disease)
Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.
familiaire ziekte van Creutzfeldt-Jakob
fCJD
Id715807002
StatusPrimitive
Associated morphologySpongy degeneration
Causative agentCreutzfeldt-Jakob agent
Finding siteBrain tissue structure
Pathological processInfectious process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetA81.0
RuleTRUE
AdviceALWAYS A81.0
CorrelationSNOMED CT source code to target map code correlation not specified