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: C0009241
Disease: Cognition Disorders
Cognition Disorders
0 47 0 0 1 2.0E-02
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome
0 7 0 0 2 0.22
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 8.3E-02
CUI: C0014175
Disease: Endometriosis
Endometriosis
0 274 0 0 1 3.6E-03
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
0 69 0 0 1 1.4E-02
CUI: C0021845
Disease: Intestinal Perforation
Intestinal Perforation
0 3 0 0 1 0.17
CUI: C0025202
Disease: melanoma
melanoma
0 515 0 0 2 3.9E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 0.25
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder
0 61 0 0 1 1.6E-02
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0 68 0 0 1 1.4E-02
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels
0 18 0 0 1 4.8E-02
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum
0 35 0 0 2 5.4E-02
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
0 64 0 0 1 1.5E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia
0 21 0 0 1 4.2E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0 663 0 0 1 1.5E-03
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
0 81 0 0 1 1.2E-02
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer
0 2 0 0 1 0.20
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0 138 0 0 1 7.1E-03
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight
0 2 0 0 1 0.20
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 2 0.29
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
0 123 0 0 1 7.9E-03
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder
0 9 0 0 1 8.3E-02
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
0 56 0 0 2 3.4E-02
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome
0 144 0 0 2 1.4E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 0.25