Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 (LGMDR3)

Alias:
Muscular Dystrophy, Limb-Girdle, Type 2d
Severe Childhood Autosomal Recessive Muscular Dystrophy
Lgmdr3
Lgmd2d
Dmda2
Severe Autosomal Recessive Muscular Dystrophy of Childhood - North African Type
Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2
Duchenne-Like Muscular Dystrophy Autosomal Recessive Type 2
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d
Dystrophy, Muscular, Limb-Girdle, Type 2d
Limb-Girdle Muscular Dystrophy 2d
Alpha-Sarcoglycanopathies
Adhalinopathy, Primary
Adhalinopathy Primary
Scarmd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3, also known as muscular dystrophy, limb-girdle, type 2d, is related to autosomal recessive limb-girdle muscular dystrophy type 2d and muscular dystrophy, limb-girdle, autosomal recessive 5. An important gene associated with Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 is SGCA (Sarcoglycan Alpha). Affiliated tissues include skeletal muscle and heart, and related phenotypes are scoliosis and congestive heart failure
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Child
--
2
19
81

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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Name
MGI
Related Gene
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Publications
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References Literature

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