Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2l

Alias:
Muscular Dystrophy, Limb-Girdle, Type 2l
Lgmd2l
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Basic Information
Medical Symptom
Gene & Mutation
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References Literature
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2l, also known as muscular dystrophy, limb-girdle, type 2l, is related to gnathodiaphyseal dysplasia and miyoshi muscular dystrophy 3, and has symptoms including myalgia An important gene associated with Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2l is ANO5 (Anoctamin 5), and among its related pathways/superpathways are DREAM Repression and Dynorphin Expression and Diseases of glycosylation. Affiliated tissues include skeletal muscle and bone, and related phenotypes are muscle and homeostasis/metabolism
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Basic Information

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Reference
MALACARDS
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Unknown
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16
125
53

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Gene & Mutation

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References Literature

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