Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency (CMS2C)

Alias:
Congenital Myasthenic Syndrome 2c
Cms2c
Myasthenic Syndrome, Congenital, Type 2c, Associated with Acetylcholine Receptor Deficiency
Congenital Myasthenic Syndrome 2c Associated with Acetylcholine Receptor Deficiency
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency, also known as congenital myasthenic syndrome 2c, is related to brain angioma and cystic lymphangioma. An important gene associated with Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency is CHRNB1 (Cholinergic Receptor Nicotinic Beta 1 Subunit), and among its related pathways/superpathways are Acetylcholine binding and downstream events and Succinylcholine Pathway, Pharmacokinetics/Pharmacodynamics. Related phenotypes are respiratory insufficiency and feeding difficulties
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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8
34
6

Medical Symptom

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Description
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Gene & Mutation

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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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