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: C0005938
Disease: Bone Density
Bone Density 		138 654 44 0.30 87 9.9E-02
CUI: C0521170
Disease: Osteoporotic Fractures
Osteoporotic Fractures 		108 40 6 3.8E-02 2 5.7E-03
CUI: C2697779
Disease: Interleukin 2 Measurement
Interleukin 2 Measurement 		5 0 2 3.5E-02 0 0
CUI: C0158447
Disease: Idiopathic osteoporosis
Idiopathic osteoporosis 		10 0 2 3.2E-02 0 0
CUI: C1832451
Disease: Cranial hyperostosis
Cranial hyperostosis 		10 0 2 3.2E-02 0 0
CUI: C4021792
Disease: Abnormality of the clavicle
Abnormality of the clavicle 		42 0 3 3.2E-02 0 0
CUI: C0271007
Disease: Phthisis bulbi
Phthisis bulbi 		11 0 2 3.2E-02 0 0
CUI: C4303510
Disease: Idiopathic premature ovarian failure
Idiopathic premature ovarian failure 		11 0 2 3.2E-02 0 0
CUI: C0268363
Disease: Osteogenesis imperfecta type IV (disorder)
Osteogenesis imperfecta type IV (disorder) 		12 0 2 3.1E-02 0 0
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		12 0 2 3.1E-02 0 0
CUI: C1835473
Disease: Diaphyseal thickening
Diaphyseal thickening 		14 0 2 3.0E-02 0 0
CUI: C3152182
Disease: Anterior chamber anomalies
Anterior chamber anomalies 		18 0 2 2.9E-02 0 0
CUI: C0339539
Disease: Familial Exudative Vitreoretinopathy
Familial Exudative Vitreoretinopathy 		19 0 2 2.8E-02 0 0
CUI: C2919755
Disease: Testicular dysgenesis syndrome
Testicular dysgenesis syndrome 		19 0 2 2.8E-02 0 0
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		56 0 3 2.8E-02 0 0
CUI: C0086395
Disease: Hearing Loss, Extreme
Hearing Loss, Extreme 		20 0 2 2.8E-02 0 0
CUI: C0581883
Disease: Complete Hearing Loss
Complete Hearing Loss 		20 0 2 2.8E-02 0 0
CUI: C0751068
Disease: Deafness, Acquired
Deafness, Acquired 		20 0 2 2.8E-02 0 0
CUI: C3665473
Disease: Bilateral Deafness
Bilateral Deafness 		20 0 2 2.8E-02 0 0
CUI: C4082305
Disease: Deaf Mutism
Deaf Mutism 		20 0 2 2.8E-02 0 0
CUI: C0011052
Disease: Prelingual Deafness
Prelingual Deafness 		22 0 2 2.7E-02 0 0
CUI: C0751254
Disease: Creutzfeldt-Jakob Disease, Familial
Creutzfeldt-Jakob Disease, Familial 		22 0 2 2.7E-02 0 0
CUI: C0235063
Disease: Respiratory Depression
Respiratory Depression 		24 0 2 2.6E-02 0 0
CUI: C4272578
Disease: Autosomal Recessive Osteopetrosis
Autosomal Recessive Osteopetrosis 		24 0 2 2.6E-02 0 0
CUI: C0265294
Disease: Pyle metaphyseal dysplasia
Pyle metaphyseal dysplasia 		25 0 2 2.6E-02 0 0