Progressive Muscular Atrophy (PMA)

Alias:
Progressive Spinal Muscular Atrophy
Pure Progressive Muscular Atrophy
Hereditary Sma - [spinal Muscle Atrophy]
Pma - [progressive Muscular Atrophy]
Progressive Spinal Muscle Atrophy
Hereditary Spinal Muscle Atrophy
Duchenne-Aran Muscle Atrophy
Progressive Muscle Atrophy
Duchenne-Aran Atrophy
Pma
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Progressive Muscular Atrophy, also known as progressive spinal muscular atrophy, is related to spinal muscular atrophy, type i and neuronopathy, distal hereditary motor, autosomal dominant 8. An important gene associated with Progressive Muscular Atrophy is CAPN3 (Calpain 3), and among its related pathways/superpathways are Neuroscience and Physico-chemical features and toxicity-associated pathways. The drugs Levetiracetam and Nootropic Agents have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and skeletal muscle, and related phenotypes are nervous system and homeostasis/metabolism
Related ID:
MESH:D009134
ICD11:1282359533

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Adult
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21
262
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Medical Symptom

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Description
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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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