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: C0152256
Disease: Disuse osteoporosis
Disuse osteoporosis 		13 0 2 0.14 0 0
CUI: C0264733
Disease: Ventricular dilatation (disorder)
Ventricular dilatation (disorder) 		13 0 2 0.14 0 0
CUI: C0340434
Disease: Dystrophic cardiomyopathy
Dystrophic cardiomyopathy 		5 0 1 0.14 0 0
CUI: C0423414
Disease: Retinal flecking
Retinal flecking 		5 0 1 0.14 0 0
CUI: C1844917
Disease: Intermittent lactic acidemia
Intermittent lactic acidemia 		5 0 1 0.14 0 0
CUI: C1849524
Disease: Pygmy (disorder)
Pygmy (disorder) 		5 0 1 0.14 0 0
CUI: C1858593
Disease: Limb-girdle muscular dystrophy, type 2E
Limb-girdle muscular dystrophy, type 2E 		5 0 1 0.14 0 0
CUI: C3203509
Disease: Neuropsychiatric syndrome
Neuropsychiatric syndrome 		6 0 1 0.12 0 0
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis 		15 0 2 0.12 0 0
CUI: C4021526
Disease: Exercise-induced rhabdomyolysis
Exercise-induced rhabdomyolysis 		6 0 1 0.12 0 0
CUI: C0268505
Disease: Ocular albinism, type II
Ocular albinism, type II 		7 0 1 0.11 0 0
CUI: C0268542
Disease: Ornithine carbamoyltransferase deficiency
Ornithine carbamoyltransferase deficiency 		17 0 2 0.11 0 0
CUI: C0398568
Disease: Blood group deletion syndrome
Blood group deletion syndrome 		7 0 1 0.11 0 0
CUI: C1282209
Disease: Choroidal neovascular membrane (disorder)
Choroidal neovascular membrane (disorder) 		7 0 1 0.11 0 0
CUI: C1328319
Disease: Ankle brachial pressure index (observable entity)
Ankle brachial pressure index (observable entity) 		7 0 1 0.11 0 0
CUI: C1859317
Disease: Cataract and cardiomyopathy
Cataract and cardiomyopathy 		7 0 1 0.11 0 0
CUI: C2720163
Disease: Placental Steroid Sulfatase Deficiency
Placental Steroid Sulfatase Deficiency 		17 0 2 0.11 0 0
CUI: C3266959
Disease: Acute focal bacterial nephritis
Acute focal bacterial nephritis 		7 0 1 0.11 0 0
CUI: C4021563
Disease: Retinal nonattachment
Retinal nonattachment 		7 0 1 0.11 0 0
CUI: C4551860
Disease: Ullrich congenital muscular dystrophy
Ullrich congenital muscular dystrophy 		7 0 1 0.11 0 0
CUI: C0268362
Disease: Osteogenesis imperfecta type III (disorder)
Osteogenesis imperfecta type III (disorder) 		18 0 2 0.11 0 0
CUI: C0154971
Disease: Presenile cataract
Presenile cataract 		8 0 1 1.0E-01 0 0
CUI: C1842914
Disease: Adult-Onset Vitelliform Macular Dystrophy
Adult-Onset Vitelliform Macular Dystrophy 		8 0 1 1.0E-01 0 0
CUI: C1855578
Disease: Exercise-induced muscle cramps
Exercise-induced muscle cramps 		8 0 1 1.0E-01 0 0
CUI: C3888099
Disease: Autosomal dominant vitreoretinochoroidopathy
Autosomal dominant vitreoretinochoroidopathy 		8 0 1 1.0E-01 0 0