muscle fiber necrosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal cell death involving muscle fibers usually associated with break in, or absence of, muscle surface fiber membrane and resulting in irreversible damage to muscle fibers. (Human Phenotype Ontology, HP_0003713)
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5 genes associated with the muscle fiber necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL6A1 collagen, type VI, alpha 1
COL6A2 collagen, type VI, alpha 2
COL6A3 collagen, type VI, alpha 3
POLG polymerase (DNA directed), gamma
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)