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: C1861980
Disease: PRENATAL CORTICAL HYPEROSTOSIS, LETHAL (disorder)
PRENATAL CORTICAL HYPEROSTOSIS, LETHAL (disorder) 		0 1 0 0 1 1.5E-02
CUI: C0231554
Disease: Osteoid formation disorder
Osteoid formation disorder 		1 0 1 5.6E-02 0 0
CUI: C0265905
Disease: Agenesis of pulmonary artery
Agenesis of pulmonary artery 		1 0 1 5.6E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 5.6E-02 0 0
CUI: C0268356
Disease: Osteogenesis imperfecta with blue sclerae AND normal teeth
Osteogenesis imperfecta with blue sclerae AND normal teeth 		1 0 1 5.6E-02 0 0
CUI: C0271149
Disease: Secondary angle-closure glaucoma
Secondary angle-closure glaucoma 		1 0 1 5.6E-02 0 0
CUI: C0271152
Disease: Malignant glaucoma
Malignant glaucoma 		1 0 1 5.6E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 5.6E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 5.6E-02 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 5.6E-02 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 1 1 5.6E-02 1 1.5E-02
CUI: C1720732
Disease: Subretinal fluid (finding)
Subretinal fluid (finding) 		1 0 1 5.6E-02 0 0
CUI: C1834345
Disease: Periosteal thickening of long tubular bones
Periosteal thickening of long tubular bones 		1 0 1 5.6E-02 0 0
CUI: C1852924
Disease: OI-EDS Combined Syndrome
OI-EDS Combined Syndrome 		1 0 1 5.6E-02 0 0
CUI: C1857034
Disease: Ehlers-Danlos syndrome, cardiac valvular form
Ehlers-Danlos syndrome, cardiac valvular form 		1 0 1 5.6E-02 0 0
CUI: C1859069
Disease: Brittle Bone Disorder
Brittle Bone Disorder 		1 0 1 5.6E-02 0 0
CUI: C1859709
Disease: Kuskokwim disease
Kuskokwim disease 		1 0 1 5.6E-02 0 0
CUI: C1970463
Disease: Type 1 collagen overmodification
Type 1 collagen overmodification 		1 0 1 5.6E-02 0 0
CUI: C2678493
Disease: BESTROPHINOPATHY
BESTROPHINOPATHY 		1 0 1 5.6E-02 0 0
CUI: C2750789
Disease: RETINITIS PIGMENTOSA, CONCENTRIC (disorder)
RETINITIS PIGMENTOSA, CONCENTRIC (disorder) 		1 0 1 5.6E-02 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 5.6E-02 0 0
CUI: C3151211
Disease: OSTEOGENESIS IMPERFECTA, TYPE X
OSTEOGENESIS IMPERFECTA, TYPE X 		1 0 1 5.6E-02 0 0
CUI: C3151218
Disease: OSTEOGENESIS IMPERFECTA, TYPE XI
OSTEOGENESIS IMPERFECTA, TYPE XI 		1 0 1 5.6E-02 0 0
CUI: C3553887
Disease: OSTEOGENESIS IMPERFECTA, TYPE XIII
OSTEOGENESIS IMPERFECTA, TYPE XIII 		1 0 1 5.6E-02 0 0
CUI: C3714945
Disease: BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16 		1 0 1 5.6E-02 0 0