Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 114548
Gene Symbol: NLRP3
NLRP3
0.130 GeneticVariation phenotype BEFREE <b>Introduction</b>: Chronic inflammatory diseases, including retinal diseases that are a major cause of vision loss, are associated with activation of the nucleotide-binding domain and leucine-rich repeat containing (NLR) protein-3 (NLRP3) inflammasome pathway. 31554417 2019
Entrez Id: 114548
Gene Symbol: NLRP3
NLRP3
0.130 AlteredExpression phenotype BEFREE Age-related macular degeneration (AMD) is a major cause of blindness in the elderly, and the activation of the NACHT, LRR, and PYD domain-containing protein 3 (NLRP3) inflammasome is involved in AMD pathogenesis. 30198786 2019
Entrez Id: 114548
Gene Symbol: NLRP3
NLRP3
0.130 GeneticVariation phenotype BEFREE Contradictory data have been presented regarding the implication of the NACHT, LRR and PYD domains-containing protein 3 (NLRP3) inflammasome in age-related macular degeneration (AMD), the leading cause of vision loss in the Western world. 29323137 2018
Entrez Id: 114548
Gene Symbol: NLRP3
NLRP3
0.130 Biomarker phenotype HPO