muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/607855
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Genes

1 genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
LAMA2 laminin, alpha 2