Atrophic Muscular Disease

Alias:
Muscular Disorders, Atrophic
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Atrophic Muscular Disease, also known as muscular disorders, atrophic, is related to glycogen storage disease v and myotonic disease. An important gene associated with Atrophic Muscular Disease is ATP2A1 (ATPase Sarcoplasmic/Endoplasmic Reticulum Ca2+ Transporting 1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Beta-Adrenergic Signaling. The drugs Pharmaceutical Solutions and glucocorticoids have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and spinal cord, and related phenotype is muscle.
Related ID:
MESH:D020966

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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8
58
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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