Myasthenic Syndrome, Congenital, 3b, Fast-Channel (CMS3B)

Alias:
Congenital Myasthenic Syndrome 3b
Cms3b
Myasthenic Syndrome, Congenital, Type 3b, Fast-Channel
Congenital Myasthenic Syndrome 3b, Fast-Channel
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myasthenic Syndrome, Congenital, 3b, Fast-Channel, is also known as congenital myasthenic syndrome 3b. An important gene associated with Myasthenic Syndrome, Congenital, 3b, Fast-Channel is CHRND (Cholinergic Receptor Nicotinic Delta Subunit). Affiliated tissues include skeletal muscle, and related phenotypes are decreased fetal movement and ptosis
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
4
5

Medical Symptom

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

Gene & Mutation

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Mutations
No data available

Related Drugs

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No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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