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Human Disease and Mouse Model Detail
Human Disease Muscular Dystrophy, Limb-Girdle, Type 2c; LGMD2C
OMIM ID: 253700
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
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models 		Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Sgcg* SGCG* View 2 models 1:1 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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Send questions and comments to User Support. 		last database update
05/22/2013
MGI 5.13 		The Jackson Laboratory