Episodic Pain Syndrome, Familial, 1 (FEPS1)

Alias:
Familial Episodic Pain Syndrome with Predominantly Upper Body Involvement
Feps1
Familial Episodic Pain Syndrome 1
Pain Syndrome, Epidosic, Familial, Type 1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Episodic Pain Syndrome, Familial, 1, also known as familial episodic pain syndrome with predominantly upper body involvement, is related to episodic pain syndrome, familial, 3 and viral laryngitis. An important gene associated with Episodic Pain Syndrome, Familial, 1 is TRPA1 (Transient Receptor Potential Cation Channel Subfamily A Member 1), and among its related pathways/superpathways are Cardiac conduction and G-Beta Gamma Signaling. Related phenotypes are episodic pain and Increased shRNA abundance (Z-score > 2)
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
8
89
1

Medical Symptom

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Description
HPO Frequency
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HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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CAS Number
Status
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No data available

Disease Model

Category
Name
MGI
Related Gene
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Publications
No data available

References Literature

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