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 3.9E-03
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 7.7E-02 0 0
CUI: C0265905
Disease: Agenesis of pulmonary artery
Agenesis of pulmonary artery 		1 0 1 7.7E-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 7.7E-02 0 0
CUI: C0332778
Disease: Diastasis, Bone
Diastasis, Bone 		1 0 1 7.7E-02 0 0
CUI: C0334393
Disease: Adenocarcinoma with squamous metaplasia
Adenocarcinoma with squamous metaplasia 		1 0 1 7.7E-02 0 0
CUI: C0409579
Disease: Rheumatic joint disease
Rheumatic joint disease 		1 0 1 7.7E-02 0 0
CUI: C0740476
Disease: Biliary carcinoma
Biliary carcinoma 		1 0 1 7.7E-02 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease 		1 0 1 7.7E-02 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 7.7E-02 0 0
CUI: C1304098
Disease: Irritant contact dermatitis due to incontinence
Irritant contact dermatitis due to incontinence 		1 0 1 7.7E-02 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 1 1 7.7E-02 1 3.9E-03
CUI: C1832942
Disease: JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1834345
Disease: Periosteal thickening of long tubular bones
Periosteal thickening of long tubular bones 		1 0 1 7.7E-02 0 0
CUI: C1849260
Disease: Facial palsy secondary to cranial hyperostosis
Facial palsy secondary to cranial hyperostosis 		1 0 1 7.7E-02 0 0
CUI: C1849263
Disease: Sclerotic scapulae
Sclerotic scapulae 		1 0 1 7.7E-02 0 0
CUI: C1849276
Disease: Cortically dense long tubular bones
Cortically dense long tubular bones 		1 0 1 7.7E-02 0 0
CUI: C1852924
Disease: OI-EDS Combined Syndrome
OI-EDS Combined Syndrome 		1 0 1 7.7E-02 0 0
CUI: C1857034
Disease: Ehlers-Danlos syndrome, cardiac valvular form
Ehlers-Danlos syndrome, cardiac valvular form 		1 0 1 7.7E-02 0 0
CUI: C1859069
Disease: Brittle Bone Disorder
Brittle Bone Disorder 		1 0 1 7.7E-02 0 0
CUI: C1970463
Disease: Type 1 collagen overmodification
Type 1 collagen overmodification 		1 0 1 7.7E-02 0 0
CUI: C3711559
Disease: Juvenile Primary Osteoporosis
Juvenile Primary Osteoporosis 		1 0 1 7.7E-02 0 0
CUI: C3806712
Disease: BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18 		1 0 1 7.7E-02 0 0
CUI: C4015948
Disease: OSTEOGENESIS IMPERFECTA, TYPE III/IV
OSTEOGENESIS IMPERFECTA, TYPE III/IV 		1 0 1 7.7E-02 0 0
CUI: C4015949
Disease: OSTEOGENESIS IMPERFECTA, TYPE IIC
OSTEOGENESIS IMPERFECTA, TYPE IIC 		1 0 1 7.7E-02 0 0