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: C0023213
Disease: Ventricular Outflow Obstruction, Left
Ventricular Outflow Obstruction, Left 		0 1 0 0 1 2.8E-03
CUI: C0272139
Disease: Erythrocytosis due to low atmospheric pressure
Erythrocytosis due to low atmospheric pressure 		0 13 0 0 2 5.5E-03
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 1.2E-02 0 0
CUI: C0021295
Disease: Infant, Premature, Diseases
Infant, Premature, Diseases 		1 0 1 1.2E-02 0 0
CUI: C0029942
Disease: Overanxious disorder
Overanxious disorder 		1 0 1 1.2E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 1.2E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 1.2E-02 0 0
CUI: C0155145
Disease: Chronic conjunctivitis
Chronic conjunctivitis 		1 0 1 1.2E-02 0 0
CUI: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse 		1 0 1 1.2E-02 0 0
CUI: C0158369
Disease: Swelling of limb
Swelling of limb 		1 0 1 1.2E-02 0 0
CUI: C0158611
Disease: Other congenital anomalies of heart
Other congenital anomalies of heart 		1 0 1 1.2E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 1.2E-02 0 0
CUI: C0178426
Disease: Oligohydramnios sequence
Oligohydramnios sequence 		1 0 1 1.2E-02 0 0
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 1.2E-02 0 0
CUI: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 1.2E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 1.2E-02 0 0
CUI: C0240211
Disease: Lip swelling
Lip swelling 		1 0 1 1.2E-02 0 0
CUI: C0263478
Disease: Ophiasis
Ophiasis 		1 0 1 1.2E-02 0 0
CUI: C0263540
Disease: Nail Loss
Nail Loss 		1 0 1 1.2E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 1.2E-02 0 0
CUI: C0264491
Disease: Acute-on-chronic respiratory failure
Acute-on-chronic respiratory failure 		1 0 1 1.2E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 1.2E-02 0 0
CUI: C0265971
Disease: Acrokeratosis Verruciformis of Hopf
Acrokeratosis Verruciformis of Hopf 		1 0 1 1.2E-02 0 0
CUI: C0268121
Disease: APRT deficiency, Japanese type
APRT deficiency, Japanese type 		1 0 1 1.2E-02 0 0
CUI: C0268396
Disease: Isolated atrial amyloid
Isolated atrial amyloid 		1 0 1 1.2E-02 0 0