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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 2.1E-02 0 0
CUI: C0029488
Disease: Other acute reactions to stress
Other acute reactions to stress 		1 0 1 2.1E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 2.1E-02 0 0
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis 		1 0 1 2.1E-02 0 0
CUI: C0232567
Disease: Hypergastrinemia
Hypergastrinemia 		1 0 1 2.1E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 2.1E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 2.1E-02 0 0
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 2.1E-02 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction 		1 0 1 2.1E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 2.1E-02 0 0
CUI: C0334483
Disease: Adult rhabdomyoma
Adult rhabdomyoma 		1 0 1 2.1E-02 0 0
CUI: C0343560
Disease: Congenital Varicella Syndrome
Congenital Varicella Syndrome 		1 0 1 2.1E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 2.1E-02 0 0
CUI: C0403647
Disease: Hypotonic bladder disorder
Hypotonic bladder disorder 		1 0 1 2.1E-02 0 0
CUI: C0472792
Disease: Hemolytic anemia due to hexokinase deficiency
Hemolytic anemia due to hexokinase deficiency 		1 0 1 2.1E-02 0 0
CUI: C0557875
Disease: Tired
Tired 		1 0 1 2.1E-02 0 0
CUI: C0741621
Disease: Brachial artery occlusion
Brachial artery occlusion 		1 0 1 2.1E-02 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 2.1E-02 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 2.1E-02 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 2.1E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 2.1E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 2.1E-02 0 0
CUI: C1263892
Disease: Neoplasm of cauda equina
Neoplasm of cauda equina 		1 0 1 2.1E-02 0 0
CUI: C1266060
Disease: Syringofibroadenoma
Syringofibroadenoma 		1 0 1 2.1E-02 0 0
CUI: C1303010
Disease: Mydriasis, Congenital
Mydriasis, Congenital 		1 0 1 2.1E-02 0 0