cachexia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease. (Human Phenotype Ontology, HP_0004326)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004326
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Genes

5 genes associated with the cachexia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ERCC4 excision repair cross-complementation group 4
MECP2 methyl CpG binding protein 2
POLG polymerase (DNA directed), gamma
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
TYMP thymidine phosphorylase