Source: INFERRED ×
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: C1854465
Disease: TUBEROUS SCLEROSIS 1 (disorder)
TUBEROUS SCLEROSIS 1 (disorder) 		0 104 0 0 2 3.9E-03
CUI: C1858674
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 		0 1 0 0 1 2.4E-03
CUI: C3806402
Disease: EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION 		0 23 0 0 2 4.6E-03
CUI: C4693362
Disease: EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2
EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2 		0 6 0 0 1 2.4E-03
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		57 0 1 7.4E-04 0 0
CUI: C0029883
Disease: Otitis Media with Effusion
Otitis Media with Effusion 		42 0 1 7.5E-04 0 0
CUI: C0032987
Disease: Ectopic Pregnancy
Ectopic Pregnancy 		41 0 1 7.5E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 7.5E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 7.5E-04 0 0
CUI: C0018810
Disease: heart rate
heart rate 		36 0 1 7.5E-04 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 0 1 7.6E-04 0 0
CUI: C0028960
Disease: Oligospermia
Oligospermia 		25 0 1 7.6E-04 0 0
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		25 0 1 7.6E-04 0 0
CUI: C0023343
Disease: Leprosy
Leprosy 		24 0 1 7.6E-04 0 0
CUI: C0233849
Disease: Personality Traits
Personality Traits 		24 0 1 7.6E-04 0 0
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		23 0 1 7.6E-04 0 0
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		23 0 1 7.6E-04 0 0
CUI: C0034088
Disease: Pulmonary Valve Insufficiency
Pulmonary Valve Insufficiency 		22 0 1 7.6E-04 0 0
CUI: C4022016
Disease: Abnormality of the preputium
Abnormality of the preputium 		22 0 1 7.6E-04 0 0
CUI: C4023917
Disease: Aplasia/Hypoplasia of the uvula
Aplasia/Hypoplasia of the uvula 		22 0 1 7.6E-04 0 0
CUI: C4025071
Disease: Aplasia/Hypoplasia of fingers
Aplasia/Hypoplasia of fingers 		22 0 1 7.6E-04 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		21 0 1 7.6E-04 0 0
CUI: C0034642
Disease: Rales
Rales 		21 0 1 7.6E-04 0 0
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		21 0 1 7.6E-04 0 0
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		21 0 1 7.6E-04 0 0