hepatic amyloidosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of amyloidosis that affects the liver. (Human Phenotype Ontology, HP_0012280)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012280
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Genes

1 genes associated with the hepatic amyloidosis 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