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: C0520798
Disease: Hepatic schistosomiasis
Hepatic schistosomiasis
4 0 1 0.14 0 0
CUI: C0549386
Disease: Sensation of warmth
Sensation of warmth
4 0 1 0.14 0 0
CUI: C0729527
Disease: Bacterial oral infection
Bacterial oral infection
4 0 1 0.14 0 0
CUI: C1096721
Disease: Neonatal Late-Onset Sepsis
Neonatal Late-Onset Sepsis
4 0 1 0.14 0 0
CUI: C1135120
Disease: Breakthrough Pain
Breakthrough Pain
4 0 1 0.14 0 0
CUI: C1334243
Disease: Intracranial Melanoma
Intracranial Melanoma
4 0 1 0.14 0 0
CUI: C2712871
Disease: Gout attack
Gout attack
4 0 1 0.14 0 0
CUI: C0034931
Disease: Reflex Sympathetic Dystrophy
Reflex Sympathetic Dystrophy
5 0 1 0.12 0 0
CUI: C0398677
Disease: Ocular sarcoidosis
Ocular sarcoidosis
5 0 1 0.12 0 0
CUI: C0475858
Disease: Generalized pruritus
Generalized pruritus
5 0 1 0.12 0 0
CUI: C1849524
Disease: Pygmy (disorder)
Pygmy (disorder)
5 0 1 0.12 0 0
CUI: C2711630
Disease: Combined immunodeficiency disease
Combined immunodeficiency disease
5 0 1 0.12 0 0
CUI: C0494491
Disease: Mononeuropathies
Mononeuropathies
6 0 1 0.11 0 0
Proliferative diabetic retinopathy - quiescent
6 0 1 0.11 0 0
CUI: C0852950
Disease: Atherosclerosis obliterans
Atherosclerosis obliterans
6 0 1 0.11 0 0
CUI: C0857493
Disease: Upper gastrointestinal symptoms
Upper gastrointestinal symptoms
6 0 1 0.11 0 0
CUI: C1323099
Disease: sympathomimetic disorder
sympathomimetic disorder
6 0 1 0.11 0 0
CUI: C3826604
Disease: Celiac disease in children
Celiac disease in children
6 0 1 0.11 0 0
CUI: C4728219
Disease: Non-proliferative retinopathy
Non-proliferative retinopathy
6 0 1 0.11 0 0
CUI: C0008439
Disease: Chondritis
Chondritis
7 0 1 1.0E-01 0 0
CUI: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia
7 0 1 1.0E-01 0 0
CUI: C0156372
Disease: Asherman Syndrome
Asherman Syndrome
7 0 1 1.0E-01 0 0
CUI: C0237326
Disease: Dyschezia
Dyschezia
7 0 1 1.0E-01 0 0
CUI: C2316401
Disease: Chronic kidney disease stage 1
Chronic kidney disease stage 1
7 0 1 1.0E-01 0 0
CUI: C0020435
Disease: Hyperbilirubinemia, Hereditary
Hyperbilirubinemia, Hereditary
8 0 1 9.1E-02 0 0