familial visceral amyloidosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050636)
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11 genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
LYZ lysozyme 1.6791
APOA2 apolipoprotein A-II 1.36727
APOA1 apolipoprotein A-I 0.94369
IGHV3-30 immunoglobulin heavy variable 3-30 0.797052
GSN gelsolin 0.693098
TTR transthyretin 0.677504
MEFV Mediterranean fever 0.409414
IAPP islet amyloid polypeptide 0.362239
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 0.297651
LPA lipoprotein, Lp(a) 0.197742
APP amyloid beta (A4) precursor protein 0.165655