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: C0009398
Disease: Color vision defect
Color vision defect 		0 4 0 0 2 0.12
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		0 4 0 0 1 5.9E-02
CUI: C0279629
Disease: Adult Acute Monoblastic Leukemia
Adult Acute Monoblastic Leukemia 		0 5 0 0 1 5.6E-02
CUI: C0279645
Disease: Childhood Acute Monoblastic Leukemia
Childhood Acute Monoblastic Leukemia 		0 5 0 0 1 5.6E-02
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 0.14
CUI: C0457334
Disease: Acute monoblastic leukemia
Acute monoblastic leukemia 		0 5 0 0 1 5.6E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 4.5E-02
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0 205 0 0 2 9.2E-03
CUI: C3272525
Disease: Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma
Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma 		0 2 0 0 2 0.14
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		0 14 0 0 2 7.7E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 1 1.4E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking 		391 765 1 2.1E-03 1 1.3E-03
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		319 0 1 2.5E-03 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 0 1 2.6E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		269 0 1 2.9E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.9E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		264 0 1 2.9E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 3.1E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		249 742 1 3.1E-03 1 1.3E-03
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		565 1138 2 3.1E-03 1 8.7E-04
CUI: C4277690
Disease: Ciliopathies
Ciliopathies 		241 0 1 3.2E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 3.2E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 3.2E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 1 3.3E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 3.4E-03 0 0