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: C1446712
Disease: Overlapping fingers
Overlapping fingers 		27 0 11 0.13 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		22 0 10 0.12 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 11 10 0.11 7 0.29
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		198 33 25 0.10 1 1.9E-02
CUI: C0409348
Disease: Flexion contracture of proximal interphalangeal joint
Flexion contracture of proximal interphalangeal joint 		168 7 22 0.10 1 3.8E-02
CUI: C1301937
Disease: Talipes
Talipes 		74 0 13 1.0E-01 0 0
CUI: C0231679
Disease: Ulnar deviation of the fingers
Ulnar deviation of the fingers 		31 0 9 9.9E-02 0 0
CUI: C0220662
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1
ARTHROGRYPOSIS, DISTAL, TYPE 1 		9 0 7 9.9E-02 0 0
CUI: C0424731
Disease: Single transverse palmar crease
Single transverse palmar crease 		78 14 13 9.7E-02 3 9.7E-02
CUI: C0265654
Disease: Tarsal Coalition
Tarsal Coalition 		22 0 8 9.6E-02 0 0
CUI: C4021735
Disease: Abnormality of the hip bone
Abnormality of the hip bone 		40 0 9 9.0E-02 0 0
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		163 0 19 8.9E-02 0 0
CUI: C1852085
Disease: Digitotalar Dysmorphism
Digitotalar Dysmorphism 		6 0 6 8.7E-02 0 0
CUI: C1862095
Disease: Bilateral single transverse palmar creases
Bilateral single transverse palmar creases 		65 0 10 8.1E-02 0 0
CUI: C1834523
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 2B
ARTHROGRYPOSIS, DISTAL, TYPE 2B 		25 0 7 8.0E-02 0 0
CUI: C0265224
Disease: Freeman-Sheldon syndrome
Freeman-Sheldon syndrome 		26 0 7 8.0E-02 0 0
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 11 7.6E-02 8 0.14
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		120 0 13 7.4E-02 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		285 44 24 7.3E-02 2 3.2E-02
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		123 10 13 7.3E-02 1 3.4E-02
CUI: C0019156
Disease: Hepatic Veno-Occlusive Disease
Hepatic Veno-Occlusive Disease 		37 0 7 7.1E-02 0 0
CUI: C1857108
Disease: Limitation of joint mobility
Limitation of joint mobility 		84 0 10 7.0E-02 0 0
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		23 4 6 7.0E-02 4 0.20
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease 		101 14 11 6.9E-02 2 6.2E-02
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		24 4 6 6.9E-02 4 0.20