Long Qt Syndrome 10 (LQT10)

Alias:
Atrial Fibrillation, Familial, 17
Lqt10
Qt Syndrome, Long, Type 10
Long Qt Syndrome-10
Atfb17
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Long Qt Syndrome 10, also known as atrial fibrillation, familial, 17, is related to second-degree atrioventricular block and diamond-blackfan anemia 3. An important gene associated with Long Qt Syndrome 10 is SCN4B (Sodium Voltage-Gated Channel Beta Subunit 4), and among its related pathways/superpathways are Transmission across Chemical Synapses and Cardiac conduction. Affiliated tissues include heart and atrioventricular node, and related phenotypes are atrial fibrillation and sudden cardiac death
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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11
92
2

Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
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Publications
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References Literature

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