Inclusion Body Myositis (IBM)

Alias:
Sporadic Inclusion Body Myositis
Ibm
Myositis, Inclusion Body
Sibm
Inclusion Body Myopathy, Autosomal Recessive
Inclusion Body Myopathy, Autosomal Dominant
Inclusion Body Myopathy, Sporadic
Myositis Inclusion Body
Nonaka Myopathy
Myositis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Inclusion Body Myositis, also known as sporadic inclusion body myositis, is related to myositis and myopathy, and has symptoms including back pain, muscle cramp and muscle rigidity. An important gene associated with Inclusion Body Myositis is GNE (Glucosamine (UDP-N-Acetyl)-2-Epimerase/N-Acetylmannosamine Kinase), and among its related pathways/superpathways are Neuroscience and miRNA role in immune response in sepsis. The drugs Titanium dioxide and Silicon have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and bone, and related phenotypes are skeletal muscle atrophy and autoimmunity
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Adult
1-9/1000000
20
279
9

Medical Symptom

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Description
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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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Name
MGI
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Publications
No data available

References Literature

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IF
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