|Name||limb girdle muscular dystrophy 1G (autosomal dominant)|
|NCBI Gene ID||553991|
|Expression in Tissues and Cell Lines||
LGMD1G has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for LGMD1G from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with LGMD1G gene/protein from the curated CTD Gene-Disease Associations dataset.|