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: C1864853
Disease: Increased vertebral height
Increased vertebral height 		7 0 3 0.14 0 0
CUI: C1865030
Disease: Hypoplastic pubic bone
Hypoplastic pubic bone 		10 0 3 0.12 0 0
CUI: C1848862
Disease: Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) 		11 0 3 0.12 0 0
CUI: C1867638
Disease: Warfarin-induced skin necrosis
Warfarin-induced skin necrosis 		2 0 2 0.11 0 0
CUI: C2678312
Disease: Three M Syndrome 1
Three M Syndrome 1 		2 0 2 0.11 0 0
CUI: C2930896
Disease: Congenital thrombotic disease, due to Protein C deficiency
Congenital thrombotic disease, due to Protein C deficiency 		2 0 2 0.11 0 0
CUI: C4021386
Disease: Abnormality of the elbow
Abnormality of the elbow 		12 0 3 0.11 0 0
CUI: C0002982
Disease: Angioid Streaks
Angioid Streaks 		13 0 3 0.11 0 0
CUI: C3806510
Disease: Horizontal ribs
Horizontal ribs 		13 0 3 0.11 0 0
CUI: C1859727
Disease: Arterial calcification of infancy
Arterial calcification of infancy 		3 0 2 0.11 0 0
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		3 0 2 0.11 0 0
CUI: C4553919
Disease: Superficial Thrombophlebitis, CTCAE
Superficial Thrombophlebitis, CTCAE 		3 0 2 0.11 0 0
CUI: C1859447
Disease: Hypoplastic ischia
Hypoplastic ischia 		14 0 3 0.10 0 0
CUI: C0263625
Disease: Subcutaneous calcification
Subcutaneous calcification 		4 0 2 1.0E-01 0 0
CUI: C2363755
Disease: Acquired Protein S Deficiency
Acquired Protein S Deficiency 		4 0 2 1.0E-01 0 0
CUI: C3536734
Disease: Hypoplastic pelvis
Hypoplastic pelvis 		15 0 3 1.0E-01 0 0
CUI: C4275075
Disease: Atypical Werner syndrome
Atypical Werner syndrome 		4 0 2 1.0E-01 0 0
CUI: C0268600
Disease: 3-methylcrotonyl CoA carboxylase 1 deficiency
3-methylcrotonyl CoA carboxylase 1 deficiency 		5 0 2 9.5E-02 0 0
CUI: C1510431
Disease: Superficial Thrombophlebitis
Superficial Thrombophlebitis 		5 0 2 9.5E-02 0 0
CUI: C1859506
Disease: Acute hyperammonemia
Acute hyperammonemia 		5 0 2 9.5E-02 0 0
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl 		5 0 2 9.5E-02 0 0
CUI: C4551505
Disease: Methylcrotonyl-CoA carboxylase deficiency
Methylcrotonyl-CoA carboxylase deficiency 		5 0 2 9.5E-02 0 0
CUI: C1856542
Disease: Prominent scalp veins
Prominent scalp veins 		6 0 2 9.1E-02 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology 		6 0 2 9.1E-02 0 0
CUI: C4022018
Disease: Telangiectasia of the skin
Telangiectasia of the skin 		56 0 6 8.8E-02 0 0