Autosomal Dominant Limb-Girdle Muscular Dystrophy

Alias:
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant
Muscular Dystrophy Limb-Girdle Autosomal Dominant
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Basic Information
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Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Dominant Limb-Girdle Muscular Dystrophy, also known as muscular dystrophy, limb-girdle, autosomal dominant, is related to muscular dystrophy, limb-girdle, type 1h and muscular dystrophy, limb-girdle, autosomal dominant 3. An important gene associated with Autosomal Dominant Limb-Girdle Muscular Dystrophy is CAPN3 (Calpain 3), and among its related pathways/superpathways are DREAM Repression and Dynorphin Expression and Cellular response to heat stress. Affiliated tissues include bone and endothelial, and related phenotypes are muscle and limbs/digits/tail
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Basic Information

Inheritance
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Prevalence
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Reference
MALACARDS
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Unknown
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17
149
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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