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: C1854684
Disease: obsolete Congenital myopia
obsolete Congenital myopia 		1 0 1 1.00 0 0
CUI: C4721549
Disease: Autosomal dominant neovascular inflammatory vitreoretinopathy
Autosomal dominant neovascular inflammatory vitreoretinopathy 		2 0 1 0.50 0 0
CUI: C0011904
Disease: Diagnostic Techniques, Cardiovascular
Diagnostic Techniques, Cardiovascular 		6 6 1 0.17 1 0.14
CUI: C0015944
Disease: Fetal Membranes, Premature Rupture
Fetal Membranes, Premature Rupture 		22 0 1 4.5E-02 0 0
CUI: C0014558
Disease: Uncinate Epilepsy
Uncinate Epilepsy 		23 0 1 4.3E-02 0 0
CUI: C0393672
Disease: Epilepsy, Benign Psychomotor, Childhood
Epilepsy, Benign Psychomotor, Childhood 		23 0 1 4.3E-02 0 0
CUI: C1142339
Disease: Intestinal adenoma
Intestinal adenoma 		23 0 1 4.3E-02 0 0
CUI: C4050064
Disease: ROSE Cluster 5
ROSE Cluster 5 		23 0 1 4.3E-02 0 0
CUI: C0948343
Disease: Transfusion-Related Acute Lung Injury
Transfusion-Related Acute Lung Injury 		24 0 1 4.2E-02 0 0
CUI: C3898147
Disease: Neonatal Hypoxic Ischemic Encephalopathy
Neonatal Hypoxic Ischemic Encephalopathy 		26 0 1 3.8E-02 0 0
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal 		29 0 1 3.4E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 3.4E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 3.4E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 3.3E-02 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 1 3.3E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 3.3E-02 0 0
CUI: C1332309
Disease: Anti-Basement Membrane Glomerulonephritis
Anti-Basement Membrane Glomerulonephritis 		39 0 1 2.6E-02 0 0
CUI: C1333296
Disease: Activated B-cell type diffuse large B-cell lymphoma
Activated B-cell type diffuse large B-cell lymphoma 		39 0 1 2.6E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 1 2.6E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 2.6E-02 0 0
CUI: C4551858
Disease: Vesicoureteral Reflux 1
Vesicoureteral Reflux 1 		47 0 1 2.1E-02 0 0
CUI: C2732618
Disease: Sessile Serrated Adenoma/Polyp
Sessile Serrated Adenoma/Polyp 		48 0 1 2.1E-02 0 0
CUI: C4049993
Disease: Aristolochic Acid Nephropathy
Aristolochic Acid Nephropathy 		49 0 1 2.0E-02 0 0
CUI: C0346989
Disease: Secondary malignant neoplasm of peritoneum
Secondary malignant neoplasm of peritoneum 		58 0 1 1.7E-02 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 1.7E-02 0 0