Fatal Familial Insomnia (FFI)

Alias:
Insomnia, Fatal Familial
Ffi
Ffi - [fatal Familial Insomnia]
Insomnia, Fatal, Familial
Insomnia Fatal Familial
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fatal Familial Insomnia, also known as insomnia, fatal familial, is related to frontotemporal lobar degeneration with tdp43 inclusions, grn-related and sleep disorder, and has symptoms including apnea, ataxia and constipation. An important gene associated with Fatal Familial Insomnia is PRNP (Prion Protein (Kanno Blood Group)), and among its related pathways/superpathways are Alzheimer's disease and miRNA effects and Neuroscience. The drugs Doxycycline and Anti-Bacterial Agents have been mentioned in the context of this disorder. Affiliated tissues include thalamus and brain, and related phenotypes are myoclonus and ataxia
Related ID:
MESH:D034062
ICD11:669154658

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
<1/1000000
20
379
53

Medical Symptom

#
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
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