amyloidosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An acquired metabolic disease that involves abnormal deposited of amyloid proteins in organs and/or tissues. (Human Disease Ontology, DOID_9120)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011034
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Genes

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

Symbol Name
APOA1 apolipoprotein A-I
APP amyloid beta (A4) precursor protein
CST3 cystatin C
FGA fibrinogen alpha chain
GSN gelsolin
IL31RA interleukin 31 receptor A
LYZ lysozyme
MEFV Mediterranean fever
NLRP3 NLR family, pyrin domain containing 3
PSEN2 presenilin 2
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A