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: C1833236
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder) 		1 0 1 0.20 0 0
CUI: C1849813
Disease: Glycogen Storage Disease of Heart, Lethal Congenital
Glycogen Storage Disease of Heart, Lethal Congenital 		1 0 1 0.20 0 0
CUI: C2936458
Disease: Fasciculoventricular Accessory Pathway
Fasciculoventricular Accessory Pathway 		1 0 1 0.20 0 0
CUI: C2936459
Disease: Nodoventricular Accessory Pathway
Nodoventricular Accessory Pathway 		1 0 1 0.20 0 0
CUI: C3539120
Disease: PROSTATE CANCER, HEREDITARY, 2
PROSTATE CANCER, HEREDITARY, 2 		1 0 1 0.20 0 0
CUI: C3809526
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17 		1 0 1 0.20 0 0
CUI: C4016809
Disease: WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET
WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET 		1 0 1 0.20 0 0
CUI: C4025004
Disease: Ventricular preexcitation with multiple accessory pathways
Ventricular preexcitation with multiple accessory pathways 		1 0 1 0.20 0 0
CUI: C4225392
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 7
COENZYME Q10 DEFICIENCY, PRIMARY, 7 		1 0 1 0.20 0 0
CUI: C0546466
Disease: Idiopathic cardiac hypertrophy
Idiopathic cardiac hypertrophy 		2 0 1 0.17 0 0
CUI: C1845864
Disease: Poor hand-eye coordination
Poor hand-eye coordination 		2 0 1 0.17 0 0
CUI: C2675179
Disease: Arginine:Glycine Amidinotransferase Deficiency
Arginine:Glycine Amidinotransferase Deficiency 		2 0 1 0.17 0 0
CUI: C3279793
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8 		2 8 1 0.17 1 0.12
CUI: C3671015
Disease: Myofiber disarray
Myofiber disarray 		2 0 1 0.17 0 0
CUI: C3825246
Disease: Diabetes in old age
Diabetes in old age 		2 0 1 0.17 0 0
CUI: C4014588
Disease: LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE
LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE 		2 0 1 0.17 0 0
CUI: C4024655
Disease: Underfolded superior helices
Underfolded superior helices 		2 0 1 0.17 0 0
CUI: C0078888
Disease: Accelerated Idioventricular Rhythm
Accelerated Idioventricular Rhythm 		3 0 1 0.14 0 0
CUI: C0151236
Disease: Conduction system abnormalities
Conduction system abnormalities 		3 0 1 0.14 0 0
CUI: C0235475
Disease: Wide QRS complex
Wide QRS complex 		3 0 1 0.14 0 0
CUI: C0238254
Disease: Metastatic Carcinoma in the Lung
Metastatic Carcinoma in the Lung 		3 0 1 0.14 0 0
CUI: C0340420
Disease: Cardiac glycogenosis
Cardiac glycogenosis 		3 0 1 0.14 0 0
CUI: C0574080
Disease: Guanidinoacetate methyltransferase deficiency
Guanidinoacetate methyltransferase deficiency 		3 0 1 0.14 0 0
CUI: C2108093
Disease: continuous electrocardiogram - paroxysmal supraventricular tachycardia
continuous electrocardiogram - paroxysmal supraventricular tachycardia 		3 0 1 0.14 0 0
CUI: C2982437
Disease: Stage II Nasopharyngeal Carcinoma AJCC v7
Stage II Nasopharyngeal Carcinoma AJCC v7 		3 0 1 0.14 0 0