Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.470 GeneticVariation GWASCAT Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. 29029846

2017
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.470 GeneticVariation GWASCAT Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. 21779176

2011
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.470 GeneticVariation GWASDB Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. 21779176

2011
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.470 GeneticVariation GWASDB This work identifies PTPRD as the fourth genome-wide significant locus for RLS. 18660810

2008
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.470 GeneticVariation GWASCAT This work identifies PTPRD as the fourth genome-wide significant locus for RLS. 18660810

2008
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.410 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683

2017
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.120 GeneticVariation GWASDB Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. 23300278

2013
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.120 GeneticVariation GWASDB Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. 21647700

2011
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.120 GeneticVariation GWASCAT A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. 20174558

2010
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.120 GeneticVariation GWASDB A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. 20174558

2010
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.110 GeneticVariation GWASCAT GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. 31311600

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.110 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.100 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.100 GeneticVariation GWASCAT GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. 31311600

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.100 GeneticVariation GWASCAT Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease. 31070104

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		0.100 GeneticVariation GWASCAT Cardiac Troponin T and Troponin I in the General Population. 31014085

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C1305855
Disease: Body mass index
Body mass index 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C4280778
Disease: Modic type vertebral endplate changes
Modic type vertebral endplate changes 		0.100 GeneticVariation GWASCAT Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes. 30808802

2019
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.100 GeneticVariation GWASCAT Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. 29531279

2018
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.100 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.100 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653

2018
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.100 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653

2018