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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 4.2E-02
CUI: C0014356
Disease: Enterocolitis
Enterocolitis 		0 2 0 0 1 5.9E-02
CUI: C0020875
Disease: Ileal Diseases
Ileal Diseases 		0 7 0 0 1 4.5E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 6.2E-02
CUI: C0036992
Disease: Short Bowel Syndrome
Short Bowel Syndrome 		0 1 0 0 1 6.2E-02
CUI: C0275551
Disease: Primary bacterial peritonitis
Primary bacterial peritonitis 		0 11 0 0 1 3.8E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 5.0E-02
CUI: C0949691
Disease: Spondylarthropathies
Spondylarthropathies 		0 7 0 0 1 4.5E-02
CUI: C1275718
Disease: Granulomatous rosacea
Granulomatous rosacea 		0 1 0 0 1 6.2E-02
CUI: C1301260
Disease: Gastrointestinal Crohn's disease
Gastrointestinal Crohn's disease 		0 2 0 0 1 5.9E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 3.6E-02
CUI: C1853438
Disease: INFLAMMATORY BOWEL DISEASE 5
INFLAMMATORY BOWEL DISEASE 5 		0 2 0 0 1 5.9E-02
CUI: C2363867
Disease: Bacterascites
Bacterascites 		0 2 0 0 1 5.9E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 6.2E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.2E-02
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
Acute Motor Axonal Neuropathy 		0 4 0 0 1 5.3E-02
CUI: C3900111
Disease: Acute motor sensory axonal neuropathy
Acute motor sensory axonal neuropathy 		0 2 0 0 1 5.9E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 5.9E-02
CUI: C4551910
Disease: Acute Inflammatory Demyelinating Polyneuropathy
Acute Inflammatory Demyelinating Polyneuropathy 		0 2 0 0 1 5.9E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 5.6E-02
CUI: C0002534
Disease: Renal Aminoacidurias
Renal Aminoacidurias 		1 0 1 9.4E-03 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 9.4E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 9.4E-03 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 9.4E-03 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 9.4E-03 0 0