type 1 muscle fiber atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophy (wasting) affecting primary type 1 muscle fibers. This feature in general can only be observed on muscle biopsy. (Human Phenotype Ontology, HP_0011807)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011807
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1 genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EMD emerin