Epilepsy, Familial Adult Myoclonic, 6 (FAME6)

Alias:
Benign Adult Familial Myoclonic Epilepsy 6
Bafme6
Fcmte6
Fame6
Cortical Myoclonic Tremor with Epilepsy, Familial, 6
Familial Adult Myoclonic Epilepsy 6
Familial Cortical Myoclonic Tremor and Epilepsy 6
Epilepsy, Myoclonic, Familial Adult, Type 6
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Epilepsy, Familial Adult Myoclonic, 6, also known as benign adult familial myoclonic epilepsy 6, is related to spinocerebellar ataxia 37 and x-linked cerebellar ataxia. An important gene associated with Epilepsy, Familial Adult Myoclonic, 6 is TNRC6A (Trinucleotide Repeat Containing Adaptor 6A). Related phenotype is myoclonic tremor.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
9
57
1

Medical Symptom

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

Gene & Mutation

#
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

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top