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: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 0.33 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 0.33 1 0.20
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 0.33 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 0.33 0 0
CUI: C0392178
Disease: Lipiduria
Lipiduria 		1 0 1 0.33 0 0
CUI: C1328928
Disease: Multiple Lentigines/LEOPARD syndrome
Multiple Lentigines/LEOPARD syndrome 		1 0 1 0.33 0 0
CUI: C1706559
Disease: Cornea verticillata
Cornea verticillata 		1 1 1 0.33 1 0.33
CUI: C1861863
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3 (disorder) 		1 7 1 0.33 1 0.11
CUI: C2678476
Disease: Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Dilated, 1y 		1 0 1 0.33 0 0
CUI: C3808145
Disease: LEFT VENTRICULAR NONCOMPACTION 9
LEFT VENTRICULAR NONCOMPACTION 9 		1 0 1 0.33 0 0
CUI: C4025162
Disease: Multiple digital exostoses
Multiple digital exostoses 		1 0 1 0.33 0 0
CUI: C4025298
Disease: Effort-induced polymorphic ventricular tachycardias
Effort-induced polymorphic ventricular tachycardias 		1 0 1 0.33 0 0
CUI: C4025818
Disease: Abnormality of skeletal maturation
Abnormality of skeletal maturation 		1 0 1 0.33 0 0
CUI: C4073188
Disease: Abnormality of the somatic nervous system
Abnormality of the somatic nervous system 		1 0 1 0.33 0 0
CUI: C0002016
Disease: Aleutian Mink Disease
Aleutian Mink Disease 		2 0 1 0.25 0 0
CUI: C0149738
Disease: neurological pain
neurological pain 		2 0 1 0.25 0 0
CUI: C0344772
Disease: Cleft leaflet of mitral valve
Cleft leaflet of mitral valve 		2 0 1 0.25 0 0
CUI: C0344975
Disease: Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Intact Ventricular Septum 		2 0 1 0.25 0 0
CUI: C0391922
Disease: Hemorrhagic enteritis
Hemorrhagic enteritis 		2 0 1 0.25 0 0
CUI: C0700199
Disease: Multiple nevi
Multiple nevi 		2 0 1 0.25 0 0
CUI: C1970820
Disease: Fabry Disease, Cardiac Variant
Fabry Disease, Cardiac Variant 		2 0 1 0.25 0 0
CUI: C3150803
Disease: NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA
NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA 		2 0 1 0.25 0 0
CUI: C3472624
Disease: B lymphoblastic leukemia lymphoma, no ICD-O subtype
B lymphoblastic leukemia lymphoma, no ICD-O subtype 		2 0 1 0.25 0 0
CUI: C0232726
Disease: Rectal tenesmus
Rectal tenesmus 		3 0 1 0.20 0 0
CUI: C0234221
Disease: Acroparesthesia
Acroparesthesia 		3 0 1 0.20 0 0