Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation disease GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation disease GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938 2013
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.500 GeneticVariation disease GWASDB A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis. 22138694 2011
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.200 GeneticVariation disease GWASDB Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. 20953186 2010
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.200 GeneticVariation disease GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.200 GeneticVariation disease GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.200 GeneticVariation disease GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088 2009
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.200 GeneticVariation disease GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.200 GeneticVariation disease GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.200 GeneticVariation disease GWASDB Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. 20598377 2010
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.200 GeneticVariation disease GWASDB Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. 20953188 2010
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.200 GeneticVariation disease GWASDB Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.200 GeneticVariation disease GWASDB Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene. 18364390 2008
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.200 GeneticVariation disease GWASDB Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. 19169254 2009
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.200 GeneticVariation disease GWASDB Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis. 17587057 2007
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.200 GeneticVariation disease GWASDB A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. 20953190 2010
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.200 GeneticVariation disease GWASDB A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. 18369459 2008
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.190 GeneticVariation disease GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946 2011
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.180 GeneticVariation disease GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.170 GeneticVariation disease GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.170 GeneticVariation disease GWASDB New loci associated with chronic hepatitis B virus infection in Han Chinese. 24162738 2013
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.160 GeneticVariation disease GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463 2014
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		0.140 GeneticVariation group GWASDB Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). 19115949 2009
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.120 GeneticVariation disease GWASDB A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. 22197929 2011
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.120 GeneticVariation disease GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805 2012