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: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 9.1E-02 0 0
CUI: C1168331
Disease: Apical myocardial infarction
Apical myocardial infarction 		1 0 1 9.1E-02 0 0
CUI: C1171363
Disease: Renoprival hypertension
Renoprival hypertension 		1 0 1 9.1E-02 0 0
CUI: C1510432
Disease: Radiation Sickness
Radiation Sickness 		1 0 1 9.1E-02 0 0
CUI: C1536651
Disease: Arterial leg ulcer
Arterial leg ulcer 		1 0 1 9.1E-02 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 9.1E-02 0 0
CUI: C1850158
Disease: Interphalangeal joint erosions
Interphalangeal joint erosions 		1 0 1 9.1E-02 0 0
CUI: C1850159
Disease: Widened metacarpal shaft
Widened metacarpal shaft 		1 0 1 9.1E-02 0 0
CUI: C1850162
Disease: Thin metatarsal cortices
Thin metatarsal cortices 		1 0 1 9.1E-02 0 0
CUI: C1860896
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6 		1 0 1 9.1E-02 0 0
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome 		1 0 1 9.1E-02 0 0
CUI: C1959587
Disease: Ventricular Free Wall Rupture
Ventricular Free Wall Rupture 		1 0 1 9.1E-02 0 0
CUI: C1963823
Disease: Hyperlipasaemia
Hyperlipasaemia 		1 0 1 9.1E-02 0 0
CUI: C2363972
Disease: Histaminosis
Histaminosis 		1 0 1 9.1E-02 0 0
CUI: C2674574
Disease: Aortic aneurysm, familial thoracic 3
Aortic aneurysm, familial thoracic 3 		1 0 1 9.1E-02 0 0
CUI: C2675128
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding) 		1 0 1 9.1E-02 0 0
CUI: C2697933
Disease: Loeys-Dietz Syndrome Type 1
Loeys-Dietz Syndrome Type 1 		1 0 1 9.1E-02 0 0
CUI: C2748355
Disease: Descending thoracic aortic dissection
Descending thoracic aortic dissection 		1 0 1 9.1E-02 0 0
CUI: C2751322
Disease: Metaphyseal Anadysplasia 2
Metaphyseal Anadysplasia 2 		1 0 1 9.1E-02 0 0
CUI: C2931588
Disease: GEMSS syndrome
GEMSS syndrome 		1 0 1 9.1E-02 0 0
CUI: C2936847
Disease: Acatalasemia Japanese type
Acatalasemia Japanese type 		1 0 1 9.1E-02 0 0
CUI: C2936848
Disease: Acatalasemia Swiss type
Acatalasemia Swiss type 		1 0 1 9.1E-02 0 0
CUI: C3280054
Disease: GELEOPHYSIC DYSPLASIA 2
GELEOPHYSIC DYSPLASIA 2 		1 0 1 9.1E-02 0 0
CUI: C3541518
Disease: ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT
ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT 		1 0 1 9.1E-02 0 0
CUI: C3714630
Disease: Respirovirus Infections
Respirovirus Infections 		1 0 1 9.1E-02 0 0