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: C0040559
Disease: Toxoplasmosis, Animal
Toxoplasmosis, Animal 		1 0 1 1.8E-02 0 0
CUI: C0042512
Disease: Ventricular Outflow Obstruction
Ventricular Outflow Obstruction 		1 0 1 1.8E-02 0 0
CUI: C0085388
Disease: Intracranial Tuberculoma
Intracranial Tuberculoma 		1 0 1 1.8E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 1.8E-02 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 1.8E-02 0 0
CUI: C0153691
Disease: Secondary malignant neoplasm of adrenal gland
Secondary malignant neoplasm of adrenal gland 		1 0 1 1.8E-02 0 0
CUI: C0155504
Disease: Serous labyrinthitis
Serous labyrinthitis 		1 0 1 1.8E-02 0 0
CUI: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery 		1 0 1 1.8E-02 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney 		1 0 1 1.8E-02 0 0
CUI: C0178426
Disease: Oligohydramnios sequence
Oligohydramnios sequence 		1 0 1 1.8E-02 0 0
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		1 0 1 1.8E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 1.8E-02 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 1.8E-02 0 0
CUI: C0235462
Disease: Anginal attack
Anginal attack 		1 0 1 1.8E-02 0 0
CUI: C0235863
Disease: Delayed delivery
Delayed delivery 		1 0 1 1.8E-02 0 0
CUI: C0238309
Disease: Ischemic peripheral neuropathy
Ischemic peripheral neuropathy 		1 0 1 1.8E-02 0 0
CUI: C0238814
Disease: brain hemangioma
brain hemangioma 		1 0 1 1.8E-02 0 0
CUI: C0240211
Disease: Lip swelling
Lip swelling 		1 0 1 1.8E-02 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		1 1 1 1.8E-02 1 0.14
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 1.8E-02 0 0
CUI: C0262568
Disease: Subendocardial myocardial infarction
Subendocardial myocardial infarction 		1 0 1 1.8E-02 0 0
CUI: C0263478
Disease: Ophiasis
Ophiasis 		1 0 1 1.8E-02 0 0
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension 		1 0 1 1.8E-02 0 0
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency 		1 0 1 1.8E-02 0 0
CUI: C0265831
Disease: Congenital absence of pulmonic valve
Congenital absence of pulmonic valve 		1 0 1 1.8E-02 0 0