Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		phenotype 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		phenotype 0.100 None 1.000 2 2 2018 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		group 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		group 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		disease 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0004106
Disease: Astigmatism
Astigmatism 		disease 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		phenotype 0.100 None 1.000 1 1 2011 2011
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0005890
Disease: Body Height
Body Height 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1305855
Disease: Body mass index
Body mass index 		phenotype 0.100 None 1.000 12 2 2010 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		phenotype 0.100 None 1.000 2 1 2010 2013
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		disease 0.120 None 1.000 0 0 2015 2017
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		disease 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		phenotype 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		group 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C4225234
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn 		disease 0.710 strong 1.000 0 1 2015 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		disease 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1834737
Disease: Cutaneous syndactyly of toes
Cutaneous syndactyly of toes 		disease 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C4024705
Disease: Decreased activity of mitochondrial complex II
Decreased activity of mitochondrial complex II 		phenotype 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C4020800
Disease: Decreased activity of mitochondrial complex IV
Decreased activity of mitochondrial complex IV 		phenotype 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1839888
Disease: Decreased activity of the pyruvate dehydrogenase complex
Decreased activity of the pyruvate dehydrogenase complex 		phenotype 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C4025022
Disease: Decreased mitochondrial complex III activity in liver tissue
Decreased mitochondrial complex III activity in liver tissue 		phenotype 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		disease 0.160 None 1.000 1 1 2013 2019