Human Disease and Mouse Model Detail
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Human Disease
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Muscular Dystrophy, Limb-Girdle, Type 2D; LGMD2D
OMIM ID: 608099
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Synonyms
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Adhalinopathy, Primary;
Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2; DMDA2
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View all models
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View ALL (2) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Sgca*
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SGCA*
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View 2 models
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1:1 Homology
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Mouse Models
Human Disease Modeled: Muscular Dystrophy, Limb-Girdle, Type 2D; LGMD2D
Associated Mouse Gene:
Sgca
Analysis Tools