Prion Disease (TSE)

Alias:
Transmissible Spongiform Encephalopathies
Transmissible Spongiform Encephalopathy
Spongiform Encephalopathy
Prion Diseases
Prion Disease Pathway
Human Transmissible Spongiform Encephalopathies, Inherited
Inherited Human Transmissible Spongiform Encephalopathies
Encephalopathy, Transmissible Spongiform
Prion Disease, Susceptibility to
Spongiform Encephalopathies
Prion-Associated Disorders
Prion-Induced Disorders
Transmissible Dementias
Prion Induced Disorder
Prion Protein Diseases
Prion Protein Disease
Human Prion Disease
Tses
Tse
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Prion Disease, also known as transmissible spongiform encephalopathies, is related to creutzfeldt-jakob disease and gerstmann-straussler disease. An important gene associated with Prion Disease is PRNP (Prion Protein (Kanno Blood Group)), and among its related pathways/superpathways are Alzheimer's disease and miRNA effects and Neuroscience. The drugs Coal tar and Quinacrine have been mentioned in the context of this disorder. Affiliated tissues include brain and cortex, and related phenotypes are nervous system and endocrine/exocrine gland
Related ID:
MESH:D017096
ICD11:1965146397

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Adult
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32
544
81

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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