Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
0 10 0 0 1 5.8E-03
CUI: C1859481
Disease: Abnormal finger flexion creases
Abnormal finger flexion creases
0 1 0 0 1 6.1E-03
CUI: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8
0 13 0 0 1 5.7E-03
Abnormality of the vertebral spinous processes
0 1 0 0 1 6.1E-03
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
1 0 1 1.1E-03 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism
1 0 1 1.1E-03 0 0
CUI: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders
1 0 1 1.1E-03 0 0
CUI: C0007279
Disease: Carotid Body Paraganglioma
Carotid Body Paraganglioma
1 0 1 1.1E-03 0 0
Diffuse Cerebral Sclerosis of Schilder
1 0 1 1.1E-03 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities
1 0 1 1.1E-03 0 0
CUI: C0013364
Disease: Dysautonomia, Familial
Dysautonomia, Familial
1 0 1 1.1E-03 0 0
CUI: C0014804
Disease: Erythromelalgia
Erythromelalgia
1 0 1 1.1E-03 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome
1 0 1 1.1E-03 0 0
Gerstmann-Straussler-Scheinker Disease
1 0 1 1.1E-03 0 0
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
1 0 1 1.1E-03 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
1 0 1 1.1E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility
1 0 1 1.1E-03 0 0
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia
1 0 1 1.1E-03 0 0
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
1 0 1 1.1E-03 0 0
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis
1 2 1 1.1E-03 2 1.2E-02
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome
1 0 1 1.1E-03 0 0
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome
1 0 1 1.1E-03 0 0
CUI: C0024748
Disease: alpha-Mannosidosis
alpha-Mannosidosis
1 0 1 1.1E-03 0 0
CUI: C0024814
Disease: Marinesco-Sjogren syndrome
Marinesco-Sjogren syndrome
1 0 1 1.1E-03 0 0
CUI: C0025210
Disease: Ocular melanosis
Ocular melanosis
1 0 1 1.1E-03 0 0