Source: ALL
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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.5E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0 306 0 0 1 1.4E-03
CUI: C0233702
Disease: Algophobia
Algophobia 		0 4 0 0 1 2.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.4E-03
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		0 24 0 0 1 2.3E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 2.5E-03
CUI: C0392156
Disease: Akathisia
Akathisia 		0 12 0 0 1 2.4E-03
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
BASAL LAMINAR DRUSEN (disorder) 		0 5 0 0 1 2.4E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 2.5E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 2.4E-03
CUI: C1720452
Disease: Soft drusen
Soft drusen 		0 5 0 0 1 2.4E-03
CUI: C1853147
Disease: MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder) 		0 5 0 0 1 2.4E-03
CUI: C2676507
Disease: Inflammatory Bowel Disease 21
Inflammatory Bowel Disease 21 		0 1 0 0 1 2.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.4E-03
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0 149 0 0 1 1.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.5E-03
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 3 7.2E-03
CUI: C4722224
Disease: Vascular Endothelial Growth Factor Receptor 2 Measurement
Vascular Endothelial Growth Factor Receptor 2 Measurement 		0 2 0 0 1 2.4E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 4.9E-03
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 1.6E-03 0 0
CUI: C0086437
Disease: Joint laxity
Joint laxity 		224 0 1 1.7E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 1 1.7E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 1.9E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 1.9E-03 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 0 1 1.9E-03 0 0