Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 (LGMDR5)

Alias:

Muscular Dystrophy, Limb-Girdle, Type 2c

Lgmdr5

Lgmd2c

Scarmd

Dmda1

Severe Autosomal Recessive Muscular Dystrophy of Childhood - North African Type

Severe Childhood Autosomal Recessive Muscular Dystrophy, North African Type

Severe Childhood Autosomal Recessive Muscular Dystrophy North African Type

Duchenne-Like Muscular Dystrophy, Autosomal Recessive, Type 1

Duchenne-Like Muscular Dystrophy Autosomal Recessive Type 1

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c

Dystrophy, Muscular, Limb-Girdle, Type 2c

Muscular Dystrophy, Duchenne-Like

Sarcoglycan, Gamma, Deficiency of

Limb-Girdle Muscular Dystrophy 2c

Adhalin Deficiency, Secondary

Sarcoglycan Gamma Deficiency

Maghrebian Myopathy

Dmda

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5, also known as muscular dystrophy, limb-girdle, type 2c, is related to autosomal recessive limb-girdle muscular dystrophy type 2c and autosomal recessive limb-girdle muscular dystrophy type 2d. An important gene associated with Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 is SGCG (Sarcoglycan Gamma). The drug Pharmaceutical Solutions has been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and lung, and related phenotypes are skeletal muscle atrophy and type 1 muscle fiber predominance

Related ID：

MALACARDS：MSC171

OMIM：253700

MESH：D049288