intercostal muscle weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of strength of the intercostal muscles, i.e., of the muscle groups running along the ribs that create and move the chest wall. (Human Phenotype Ontology, HP_0004878)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004878
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Genes

1 genes associated with the intercostal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TRPV4 transient receptor potential cation channel, subfamily V, member 4