Creutzfeldt-Jakob Disease (CJD)

Alias:
Variant Creutzfeldt-Jakob Disease
Inherited Creutzfeldt-Jakob Disease
Bovine Spongiform Encephalopathy
Vcjd
Cjd
Creutzfeldt-Jakob Disease, Familial
Encephalopathy, Bovine Spongiform
Variant Mcj
Creutzfeldt-Jakob Disease, Variant, Resistance to
Vcjd - [variant Creutzfeldt-Jakob Disease]
New Variant Creutzfeldt-Jakob Disease
Creutzfeldt-Jakob Disease, Sporadic
Creutzfeldt-Jakob Disease, Variant
Subacute Spongiform Encephalopathy
Acquired Creutzfeldt-Jakob Disease
Familial Creutzfeldt-Jakob Disease
Encephalopathy Bovine Spongiform
Transmissible Virus Dementia
Creutzfeldt Jacob Syndrome
Creutzfeldt-Jakob Syndrome
Creutzfeldt Jakob Disease
Creutzfeldt-Jacob Disease
Jakob-Creutzfeldt Disease
Creutzfeldt Jacob Disease
Inherited Cjd
Acquired Cjd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Creutzfeldt-Jakob Disease, also known as variant creutzfeldt-jakob disease, is related to gerstmann-straussler disease and normal pressure hydrocephalus, and has symptoms including back pain, headache and hemiparesis. An important gene associated with Creutzfeldt-Jakob Disease is PRNP (Prion Protein (Kanno Blood Group)), and among its related pathways/superpathways are Neuroscience and Neural Stem Cells and Lineage-specific Markers. The drugs Coal tar and Quinacrine have been mentioned in the context of this disorder. Affiliated tissues include brain and spinal cord, and related phenotypes are seizure and abnormal pyramidal sign
Related ID:
MESH:D007562
ICD11:378572696

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
45
666
132

Medical Symptom

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Description
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Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
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Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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