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: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 0.17 0 0
CUI: C0238110
Disease: Chronic epididymitis
Chronic epididymitis 		1 0 1 0.17 0 0
CUI: C0267896
Disease: Mucocele of gallbladder
Mucocele of gallbladder 		1 0 1 0.17 0 0
CUI: C0344544
Disease: Polycoria
Polycoria 		1 0 1 0.17 0 0
CUI: C0399356
Disease: Supernumerary cusp
Supernumerary cusp 		1 0 1 0.17 0 0
CUI: C0948393
Disease: Oedematous pancreatitis
Oedematous pancreatitis 		1 0 1 0.17 0 0
CUI: C1274923
Disease: Cutaneous hyperalgesia
Cutaneous hyperalgesia 		1 0 1 0.17 0 0
CUI: C1838049
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 1
Epilepsy, Nocturnal Frontal Lobe, Type 1 		1 0 1 0.17 0 0
CUI: C1862376
Disease: Abnormally prominent line of Schwalbe
Abnormally prominent line of Schwalbe 		1 0 1 0.17 0 0
CUI: C2751831
Disease: Myopathy, Myofibrillar, Bag3-Related
Myopathy, Myofibrillar, Bag3-Related 		1 0 1 0.17 0 0
CUI: C3151293
Disease: CARDIOMYOPATHY, DILATED, 1HH
CARDIOMYOPATHY, DILATED, 1HH 		1 0 1 0.17 0 0
CUI: C3249879
Disease: Combat Fatigue
Combat Fatigue 		1 0 1 0.17 0 0
CUI: C3266628
Disease: Persistent asthma
Persistent asthma 		1 0 1 0.17 0 0
CUI: C4016279
Disease: LEPTIN DYSFUNCTION
LEPTIN DYSFUNCTION 		1 0 1 0.17 0 0
CUI: C4310930
Disease: ANTERIOR SEGMENT DYSGENESIS 4, PETERS ANOMALY SUBTYPE
ANTERIOR SEGMENT DYSGENESIS 4, PETERS ANOMALY SUBTYPE 		1 0 1 0.17 0 0
CUI: C4476718
Disease: Abnormality of the corneal limbus
Abnormality of the corneal limbus 		1 0 1 0.17 0 0
CUI: C4703706
Disease: Conjunctival dermolipoma
Conjunctival dermolipoma 		1 0 1 0.17 0 0
CUI: C0013375
Disease: Dysganglionosis
Dysganglionosis 		2 0 1 0.14 0 0
CUI: C0266752
Disease: Twin placenta
Twin placenta 		2 0 1 0.14 0 0
CUI: C0431649
Disease: Vaginal septum
Vaginal septum 		2 0 1 0.14 0 0
CUI: C0544669
Disease: Hypomanic personality
Hypomanic personality 		2 0 1 0.14 0 0
CUI: C1275047
Disease: Radiation-induced xerostomia
Radiation-induced xerostomia 		2 0 1 0.14 0 0
CUI: C1842031
Disease: IRIDOGONIODYSGENESIS, TYPE 2
IRIDOGONIODYSGENESIS, TYPE 2 		2 0 1 0.14 0 0
CUI: C1854335
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 3
Epilepsy, Nocturnal Frontal Lobe, Type 3 		2 0 1 0.14 0 0
CUI: C1867155
Disease: RING DERMOID OF CORNEA
RING DERMOID OF CORNEA 		2 0 1 0.14 0 0