Febrile Seizures, Familial, 9 (FEB9)

Alias:
Febrile Convulsions, Familial, 9
Familial Febrile Seizures 9
Feb9
Familial Febrile Convulsions 9
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Febrile Seizures, Familial, 9, also known as febrile convulsions, familial, 9, is related to partial motor epilepsy and developmental and epileptic encephalopathy 74. An important gene associated with Febrile Seizures, Familial, 9 is FEB9 (Febrile Convulsions, Familial, 9), and among its related pathways/superpathways are NF-kappaB Pathway and Prader-Willi and Angelman syndrome. Related phenotypes are generalized non-motor (absence) seizure and eeg with spike-wave complexes (>3.5 hz)

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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8
74
1

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
No data available

References Literature

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