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Human Disease and Mouse Model Detail
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| Human Disease | Term: Muscular Dystrophy, Limb-Girdle, Type 2c; LGMD2C |
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| Synonyms | Adhalin Deficiency, Secondary; DMDA; Duchenne-Like Muscular Dystrophy, Autosomal Recessive, Type 1; DMDA1; Maghrebian Myopathy; Muscular Dystrophy, Duchenne-Like; Sarcoglycan, Gamma, Deficiency of; Severe Childhood Autosomal Recessive Muscular Dystrophy, North African Type; SCARMD | ||||||||||||||||||||||||
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
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Mouse Models |
1Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes. |
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 04/03/2013 MGI 5.12 |
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Analysis Tools
...both mouse and human orthologous genes.