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: C0267809
Disease: Cirrhosis, Cryptogenic
Cirrhosis, Cryptogenic 		15 5 7 1.6E-02 2 1.0E-01
CUI: C0553730
Disease: Calcium pyrophosphate deposition disease
Calcium pyrophosphate deposition disease 		34 5 2 4.3E-03 2 1.0E-01
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait 		34 5 9 2.0E-02 2 1.0E-01
CUI: C1698259
Disease: HCV coinfection
HCV coinfection 		37 5 15 3.3E-02 2 1.0E-01
CUI: C0014173
Disease: Endometrial Hyperplasia
Endometrial Hyperplasia 		143 6 33 6.1E-02 2 9.5E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 1 2.3E-03 2 9.5E-02
CUI: C0032708
Disease: Disorders of Porphyrin Metabolism
Disorders of Porphyrin Metabolism 		26 7 6 1.3E-02 2 9.1E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		96 8 3 5.7E-03 2 8.7E-02
CUI: C2931689
Disease: Dystrophia myotonica 2
Dystrophia myotonica 2 		118 21 34 6.6E-02 3 8.6E-02
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		67 9 15 3.1E-02 2 8.3E-02
CUI: C0022408
Disease: Arthropathy
Arthropathy 		187 10 40 6.9E-02 2 8.0E-02
CUI: C1384584
Disease: Generalized osteoarthritis
Generalized osteoarthritis 		63 10 13 2.7E-02 2 8.0E-02
CUI: C0002893
Disease: Refractory anemias
Refractory anemias 		340 11 65 9.2E-02 2 7.7E-02
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		22 11 4 8.8E-03 2 7.7E-02
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia 		88 11 14 2.8E-02 2 7.7E-02
CUI: C0030286
Disease: Pancreatic Diseases
Pancreatic Diseases 		100 11 26 5.1E-02 2 7.7E-02
CUI: C0751955
Disease: Brain Infarction
Brain Infarction 		114 11 28 5.4E-02 2 7.7E-02
CUI: C0403447
Disease: Chronic Kidney Insufficiency
Chronic Kidney Insufficiency 		52 12 16 3.4E-02 2 7.4E-02
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis 		63 12 14 2.9E-02 2 7.4E-02
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		226 28 43 7.0E-02 3 7.1E-02
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 13 4 8.3E-03 2 7.1E-02
CUI: C0240066
Disease: Iron deficiency
Iron deficiency 		179 13 28 4.8E-02 2 7.1E-02
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		218 60 66 0.11 5 6.9E-02
CUI: C0279607
Disease: Adult Hepatocellular Carcinoma
Adult Hepatocellular Carcinoma 		150 14 37 6.8E-02 2 6.9E-02
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
MYOTONIC DYSTROPHY 1 		179 14 37 6.4E-02 2 6.9E-02