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: C0080310
Disease: Left Ventricular Function
Left Ventricular Function 		1 0 1 0.50 0 0
CUI: C0474355
Disease: Peripheral retinal neovascularization
Peripheral retinal neovascularization 		1 0 1 0.50 0 0
CUI: C1854684
Disease: obsolete Congenital myopia
obsolete Congenital myopia 		1 0 1 0.50 0 0
CUI: C4024803
Disease: Posterior retinal neovascularization
Posterior retinal neovascularization 		1 0 1 0.50 0 0
CUI: C4024820
Disease: Large hyperpigmented retinal spots
Large hyperpigmented retinal spots 		1 0 1 0.50 0 0
CUI: C0011904
Disease: Diagnostic Techniques, Cardiovascular
Diagnostic Techniques, Cardiovascular 		6 0 1 0.14 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 2 1 8.3E-02 1 0.50
CUI: C0042909
Disease: Vitreous Hemorrhage
Vitreous Hemorrhage 		12 0 1 7.7E-02 0 0
CUI: C1869123
Disease: Limb-girdle muscular dystrophy type 2A
Limb-girdle muscular dystrophy type 2A 		18 0 1 5.3E-02 0 0
CUI: C0344290
Disease: Vitreoretinal degeneration
Vitreoretinal degeneration 		20 0 1 4.8E-02 0 0
CUI: C0011876
Disease: Cataract due to diabetes mellitus
Cataract due to diabetes mellitus 		22 0 1 4.3E-02 0 0
CUI: C0015944
Disease: Fetal Membranes, Premature Rupture
Fetal Membranes, Premature Rupture 		22 0 1 4.3E-02 0 0
CUI: C0014558
Disease: Uncinate Epilepsy
Uncinate Epilepsy 		23 0 1 4.2E-02 0 0
CUI: C0393672
Disease: Epilepsy, Benign Psychomotor, Childhood
Epilepsy, Benign Psychomotor, Childhood 		23 0 1 4.2E-02 0 0
CUI: C1142339
Disease: Intestinal adenoma
Intestinal adenoma 		23 0 1 4.2E-02 0 0
CUI: C4050064
Disease: ROSE Cluster 5
ROSE Cluster 5 		23 0 1 4.2E-02 0 0
CUI: C0948343
Disease: Transfusion-Related Acute Lung Injury
Transfusion-Related Acute Lung Injury 		24 0 1 4.0E-02 0 0
CUI: C3898147
Disease: Neonatal Hypoxic Ischemic Encephalopathy
Neonatal Hypoxic Ischemic Encephalopathy 		26 0 1 3.7E-02 0 0
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal 		29 0 1 3.3E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 3.3E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 3.3E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 3.2E-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 3.2E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 3.2E-02 0 0
CUI: C3888523
Disease: Autoimmune uveitis
Autoimmune uveitis 		31 0 1 3.1E-02 0 0