Myasthenic Syndrome, Congenital, 1b, Fast-Channel (CMS1B)

Alias:
Cms1b
Myasthenic Syndrome, Congenital, Fast-Channel
Congenital Myasthenic Syndrome 1b
Myasthenic Syndrome, Congenital, Type 1b, Fast-Channel
Congenital Myasthenic Syndrome 1b, Fast-Channel
Myasthenic Syndrome, Fast-Channel Congenital
Congenital Myasthenic Syndrome Ib
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myasthenic Syndrome, Congenital, 1b, Fast-Channel, also known as cms1b, is related to myasthenic syndrome, congenital, 10 and myasthenic syndrome, congenital, 4b, fast-channel, and has symptoms including facial paresis An important gene associated with Myasthenic Syndrome, Congenital, 1b, Fast-Channel is CHRNA1 (Cholinergic Receptor Nicotinic Alpha 1 Subunit), and among its related pathways/superpathways are Statin Pathway - Generalized, Pharmacokinetics and Blood-Brain Barrier and Immune Cell Transmigration: Overview. Affiliated tissues include skeletal muscle and brain, and related phenotypes are easy fatigability and neck muscle weakness
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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17
111
7

Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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