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Human Disease and Mouse Model Detail
Human Disease Muscular Dystrophy, Limb-Girdle, Type 2c; LGMD2C
OMIM ID: 253700
Human Phenotype Ontology associations
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     SGCG* Sgcg* View 2 models HomoloGene and HGNC
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
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last database update
MGI 6.07
The Jackson Laboratory