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: C3495566
Disease: Reflux nephropathy (disorder)
Reflux nephropathy (disorder) 		13 0 2 7.7E-02 0 0
CUI: C0586358
Disease: Biliary Intraepithelial Neoplasia
Biliary Intraepithelial Neoplasia 		14 0 2 7.4E-02 0 0
CUI: C1812607
Disease: Aortic aneurysm and dissection
Aortic aneurysm and dissection 		14 0 2 7.4E-02 0 0
CUI: C0220666
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA 		15 0 2 7.1E-02 0 0
CUI: C0042420
Disease: Vasovagal syncope
Vasovagal syncope 		16 0 2 6.9E-02 0 0
CUI: C3161650
Disease: Primary immunoglobulin A nephropathy (disorder)
Primary immunoglobulin A nephropathy (disorder) 		16 0 2 6.9E-02 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever 		1 0 1 6.7E-02 0 0
CUI: C0085426
Disease: Gram-Positive Bacterial Infections
Gram-Positive Bacterial Infections 		17 0 2 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