You are using an outdated browser. Please upgrade your browser to improve your experience.
Limb-girdle muscular dystrophy 1B
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description An autosomal dominant degenerative myopathy with age-related atrioventricular cardiac conduction disturbances, dilated cardiomyopathy, and the absence of early contractures. Characterized by slowly progressive skeletal muscle weakness of the hip and shoulder girdles. Muscle biopsy shows mild dystrophic changes.
DataSource References
UniProt Disease: OMIM:159001
Use Cases
Submit Feedback
Download Data for Limb-girdle muscular dystrophy 1B
data still loading...
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
UniProt Disease
High level summary of knowledge for a disease, including descriptions and datasource references.