abnormality of the fascia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of fascia. (Human Phenotype Ontology, HP_0100536)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100536
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1 genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A