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: C0007166
Disease: Low Cardiac Output
Low Cardiac Output 		1 0 1 1.7E-02 0 0
CUI: C0020683
Disease: Hypovolemic Shock
Hypovolemic Shock 		1 0 1 1.7E-02 0 0
CUI: C0029897
Disease: Otorhinolaryngologic Neoplasms
Otorhinolaryngologic Neoplasms 		1 0 1 1.7E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 1.7E-02 0 0
CUI: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery 		1 0 1 1.7E-02 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney 		1 0 1 1.7E-02 0 0
CUI: C0233525
Disease: Defensive aggression
Defensive aggression 		1 0 1 1.7E-02 0 0
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension 		1 0 1 1.7E-02 0 0
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency 		1 0 1 1.7E-02 0 0
CUI: C0266284
Disease: Lingual Thyroid
Lingual Thyroid 		1 0 1 1.7E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 1.7E-02 0 0
CUI: C0270411
Disease: Mild mood disorder
Mild mood disorder 		1 0 1 1.7E-02 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 1.7E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 1.7E-02 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 1.7E-02 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 1.7E-02 0 0
CUI: C0272356
Disease: von Willebrand disease, type IID
von Willebrand disease, type IID 		1 0 1 1.7E-02 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 1.7E-02 0 0
CUI: C0334689
Disease: C cell tumor
C cell tumor 		1 0 1 1.7E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 1.7E-02 0 0
CUI: C0342394
Disease: Familial central diabetes insipidus
Familial central diabetes insipidus 		1 0 1 1.7E-02 0 0
CUI: C0398610
Disease: Congenital von Willebrand's disease
Congenital von Willebrand's disease 		1 0 1 1.7E-02 0 0
CUI: C0406563
Disease: Follicular atrophoderma
Follicular atrophoderma 		1 0 1 1.7E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 1.7E-02 0 0
CUI: C0477633
Disease: Cervical disc disorder
Cervical disc disorder 		1 0 1 1.7E-02 0 0