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: C0001811
Disease: Aging
Aging 		1 0 1 1.6E-03 0 0
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections 		1 0 1 1.6E-03 0 0
CUI: C0022350
Disease: Jaundice, Chronic Idiopathic
Jaundice, Chronic Idiopathic 		1 0 1 1.6E-03 0 0
CUI: C0024441
Disease: Macular Holes
Macular Holes 		1 0 1 1.6E-03 0 0
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		1 0 1 1.6E-03 0 0
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		1 0 1 1.6E-03 0 0
CUI: C0034091
Disease: Pulmonary Veno-Occlusive Disease (disorder)
Pulmonary Veno-Occlusive Disease (disorder) 		1 0 1 1.6E-03 0 0
CUI: C0038355
Disease: Stomach Diverticulum
Stomach Diverticulum 		1 0 1 1.6E-03 0 0
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		1 0 1 1.6E-03 0 0
CUI: C0149756
Disease: Fasciitis, Plantar
Fasciitis, Plantar 		1 0 1 1.6E-03 0 0
CUI: C0155883
Disease: Chronic obstructive asthma (with obstructive pulmonary disease)
Chronic obstructive asthma (with obstructive pulmonary disease) 		1 0 1 1.6E-03 0 0
CUI: C0158360
Disease: Fibromatosis, Plantar
Fibromatosis, Plantar 		1 0 1 1.6E-03 0 0
CUI: C0158611
Disease: Other congenital anomalies of heart
Other congenital anomalies of heart 		1 0 1 1.6E-03 0 0
CUI: C0202071
Disease: Homovanillic acid measurement
Homovanillic acid measurement 		1 0 1 1.6E-03 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 1.6E-03 0 0
CUI: C0240709
Disease: Pericardial constriction
Pericardial constriction 		1 0 1 1.6E-03 0 0
CUI: C0265211
Disease: Marshall-Smith syndrome
Marshall-Smith syndrome 		1 0 1 1.6E-03 0 0
CUI: C0265235
Disease: Marshall syndrome
Marshall syndrome 		1 0 1 1.6E-03 0 0
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		1 0 1 1.6E-03 0 0
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		1 0 1 1.6E-03 0 0
CUI: C0265971
Disease: Acrokeratosis Verruciformis of Hopf
Acrokeratosis Verruciformis of Hopf 		1 0 1 1.6E-03 0 0
CUI: C0268247
Disease: Niemann-Pick Disease, Type D
Niemann-Pick Disease, Type D 		1 0 1 1.6E-03 0 0
CUI: C0268425
Disease: Alstrom Syndrome
Alstrom Syndrome 		1 0 1 1.6E-03 0 0
CUI: C0268575
Disease: Isovaleryl-CoA dehydrogenase deficiency
Isovaleryl-CoA dehydrogenase deficiency 		1 0 1 1.6E-03 0 0
CUI: C0271198
Disease: Scotoma, Arcuate
Scotoma, Arcuate 		1 0 1 1.6E-03 0 0