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: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever 		1 0 1 6.7E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 6.7E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 6.7E-02 0 0
CUI: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery 		1 0 1 6.7E-02 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney 		1 0 1 6.7E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 6.7E-02 0 0
CUI: C0201896
Disease: Arylsulfatase B measurement
Arylsulfatase B measurement 		1 0 1 6.7E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 6.7E-02 0 0
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension 		1 0 1 6.7E-02 0 0
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency 		1 0 1 6.7E-02 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 6.7E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 6.7E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 6.7E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 6.7E-02 0 0
CUI: C0268218
Disease: Maroteaux-Lamy syndrome, mild form
Maroteaux-Lamy syndrome, mild form 		1 0 1 6.7E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 6.7E-02 0 0
CUI: C0521623
Disease: Kidney crystallization
Kidney crystallization 		1 0 1 6.7E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 6.7E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 6.7E-02 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease 		1 0 1 6.7E-02 0 0
CUI: C0877138
Disease: Osteopenia periarticular
Osteopenia periarticular 		1 0 1 6.7E-02 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 6.7E-02 0 0
CUI: C1301626
Disease: Hypertension with albuminuria
Hypertension with albuminuria 		1 0 1 6.7E-02 0 0
CUI: C1328928
Disease: Multiple Lentigines/LEOPARD syndrome
Multiple Lentigines/LEOPARD syndrome 		1 0 1 6.7E-02 0 0
CUI: C1832942
Disease: JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder) 		1 0 1 6.7E-02 0 0