| Human Disease |
Term: Muscular Dystrophy, Limb-Girdle, Type 1B; LGMD1B
OMIM ID: 159001
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| Synonyms |
Muscular Dystrophy, Proximal, Type 1B |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
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Characteristics of this human disease are associated with mutations in... |
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 ...the mouse gene.
OMIM data currently do not associate this disease with the orthologous human gene. |
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 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
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Mouse Models
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1Human genes are associated with this disease. Mouse model genotypes do not include mutations in the orthologs of these human genes.
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Analysis Tools