Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0002871
Disease: Anemia
Anemia 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0031256
Disease: Petechiae
Petechiae 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0151526
Disease: Premature Birth
Premature Birth 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0751740
Disease: Lenticulostriate Vasculopathy
Lenticulostriate Vasculopathy 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C2973725
Disease: Pulmonary arterial hypertension
Pulmonary arterial hypertension 		0.100 CausalMutation CLINVAR An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1. 30965144

2020
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.100 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.100 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.100 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.100 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement 		0.100 GeneticVariation GWASDB Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. 21829393

2011
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0202083
Disease: Immunoglobulin A measurement
Immunoglobulin A measurement 		0.100 GeneticVariation GWASDB Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. 20694011

2010
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.100 GeneticVariation GWASCAT Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. 20694011

2010
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0003486
Disease: Aortic Aneurysm
Aortic Aneurysm 		0.100 Biomarker HPO

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		0.100 Biomarker HPO

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0004368
Disease: Autoimmune state
Autoimmune state 		0.100 Biomarker HPO

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 Biomarker HPO

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		0.100 Biomarker HPO

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0008058
Disease: Chilblains
Chilblains 		0.100 Biomarker HPO

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0009024
Disease: Clonus
Clonus 		0.100 GeneticVariation CLINVAR

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.100 Biomarker HPO

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C0011334
Disease: Dental caries
Dental caries 		0.100 Biomarker HPO