Intermediate Nemaline Myopathy

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Intermediate Nemaline Myopathy is related to congenital myopathy 4a, autosomal dominant and nemaline myopathy 10. An important gene associated with Intermediate Nemaline Myopathy is ACTA1 (Actin Alpha 1, Skeletal Muscle), and among its related pathways/superpathways are Cardiac conduction and Striated muscle contraction pathway. Affiliated tissues include skeletal muscle, and related phenotypes are nemaline bodies and severe muscular hypotonia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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4
25
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Medical Symptom

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Categorization
Description
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No data available

Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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