About   Help   FAQ
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; Muscular Dystrophy, Limb-Girdle; 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
References Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/18/2014
MGI 5.20
The Jackson Laboratory