Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes
0 31 0 0 1 2.0E-02
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
0 45 0 0 1 1.6E-02
CUI: C0019348
Disease: Herpes Simplex Infections
Herpes Simplex Infections
0 11 0 0 1 3.4E-02
Gamma glutamyl transferase measurement
0 7 0 0 1 4.0E-02
Familial hypercholesterolemia - heterozygous
0 34 0 0 1 1.9E-02
CUI: C0523509
Disease: Apolipoprotein B Assay
Apolipoprotein B Assay
0 2 0 0 1 5.0E-02
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
0 25 0 0 1 2.3E-02
Serum gamma-glutamyl transferase measurement
0 108 0 0 1 7.9E-03
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
Alzheimer disease, familial, type 3
0 124 0 0 1 7.0E-03
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis
1 0 1 5.0E-02 0 0
CUI: C0393890
Disease: Suprascapular nerve compression
Suprascapular nerve compression
1 0 1 5.0E-02 0 0
CUI: C0858613
Disease: Optic nerve oedema
Optic nerve oedema
1 0 1 5.0E-02 0 0
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4
1 0 1 5.0E-02 0 0
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
1 0 1 5.0E-02 0 0
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
1 0 1 5.0E-02 0 0
SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
1 0 1 5.0E-02 0 0
CUI: C4049395
Disease: Chronic hepatitis C genotype 2
Chronic hepatitis C genotype 2
1 0 1 5.0E-02 0 0
CUI: C4225298
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 104
DEAFNESS, AUTOSOMAL RECESSIVE 104
1 0 1 5.0E-02 0 0
ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS
1 0 1 5.0E-02 0 0
CUI: C0024528
Disease: Malaise and fatigue
Malaise and fatigue
2 0 1 4.8E-02 0 0
CUI: C0494479
Disease: Other headache syndrome
Other headache syndrome
2 0 1 4.8E-02 0 0
CUI: C1367972
Disease: Phlebitis and thrombophlebitis
Phlebitis and thrombophlebitis
2 0 1 4.8E-02 0 0
CUI: C1619716
Disease: Cystatin C measurement
Cystatin C measurement
2 0 1 4.8E-02 0 0
CUI: C1836824
Disease: Amish Infantile Epilepsy Syndrome
Amish Infantile Epilepsy Syndrome
2 0 1 4.8E-02 0 0
CUI: C3888909
Disease: BAFF polymorphism
BAFF polymorphism
2 0 1 4.8E-02 0 0