Myasthenic Syndrome, Congenital, 7b, Presynaptic, Autosomal Recessive (CMS7B)

Alias:
Cms7b
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myasthenic Syndrome, Congenital, 7b, Presynaptic, Autosomal Recessive, is also known as cms7b. An important gene associated with Myasthenic Syndrome, Congenital, 7b, Presynaptic, Autosomal Recessive is SYT2 (Synaptotagmin 2). Affiliated tissues include tongue and eye, and related phenotypes are hypotonia and weakness of facial musculature
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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
8
4

Medical Symptom

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Categorization
Description
HPO Frequency
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No data available

Gene & Mutation

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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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