limb-girdle muscular dystrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A muscular dystrophy that is characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles. (Human Disease Ontology, DOID_11724)
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3 genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HNRNPDL heterogeneous nuclear ribonucleoprotein D-like
LMNA lamin A/C
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)