skeletal muscle endomysial fibrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description replacement of the layer of connective tissue that ensheaths a muscle fiber by fibrous tissue resulting in separation of individual fibers (Mammalian Phenotype Ontology, MP_0009420)
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5 gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DMD dystrophin
DYSF dysferlin
LAMA2 laminin, alpha 2
LARGE like-glycosyltransferase
VCP valosin containing protein