PLA2G5, phospholipase A2 group V, 5322

N. diseases: 29; N. variants: 15
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3714514
Disease: Infection
Infection
0.020 Biomarker group LHGDN Group V and X secretory phospholipase A2 prevents adenoviral infection in mammalian cells. 16146426 2006
CUI: C0016059
Disease: Fibrosis
Fibrosis
0.010 AlteredExpression phenotype LHGDN Distribution of type V secretory phospholipase A2 expression in human hepatocytes damaged by liver disease. 15377291 2004
CUI: C0023895
Disease: Liver diseases
Liver diseases
0.010 Biomarker group LHGDN Distribution of type V secretory phospholipase A2 expression in human hepatocytes damaged by liver disease. 15377291 2004
CUI: C1856718
Disease: Fleck Retina, Familial Benign
Fleck Retina, Familial Benign
0.700 GermlineCausalMutation disease ORPHANET Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retina. 22137173 2011
CUI: C1856718
Disease: Fleck Retina, Familial Benign
Fleck Retina, Familial Benign
0.700 GeneticVariation disease UNIPROT Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retina. 22137173 2011
CUI: C1856718
Disease: Fleck Retina, Familial Benign
Fleck Retina, Familial Benign
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
0.300 Biomarker group GENOMICS_ENGLAND
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
0.300 Biomarker group GENOMICS_ENGLAND
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
0.300 Biomarker group GENOMICS_ENGLAND
Low density lipoprotein cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012