Hyaline Body Myopathy

Alias:
Myosin Storage Myopathy
Autosomal Dominant Hyaline Body Myopathy
Myopathy, Myosin Storage
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyaline Body Myopathy, also known as myosin storage myopathy, is related to congenital myopathy 7a, myosin storage, autosomal dominant and congenital myopathy 7b, myosin storage, autosomal recessive, and has symptoms including waddling gait An important gene associated with Hyaline Body Myopathy is MYH7 (Myosin Heavy Chain 7), and among its related pathways/superpathways are PAK Pathway and Sweet Taste Signaling. The drugs Salbutamol and Tocolytic Agents have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, and related phenotypes are muscle and growth/size/body region
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Unknown
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Medical Symptom

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

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
Related Gene
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Publications
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References Literature

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