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: C0220662
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1
ARTHROGRYPOSIS, DISTAL, TYPE 1 		9 0 8 0.30 0 0
CUI: C1852085
Disease: Digitotalar Dysmorphism
Digitotalar Dysmorphism 		6 0 6 0.23 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		22 15 8 0.20 2 0.11
CUI: C4021959
Disease: Round ear
Round ear 		10 0 5 0.16 0 0
CUI: C1834523
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 2B
ARTHROGRYPOSIS, DISTAL, TYPE 2B 		25 6 7 0.16 1 9.1E-02
CUI: C3280526
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1B
ARTHROGRYPOSIS, DISTAL, TYPE 1B 		4 0 4 0.15 0 0
CUI: C0231678
Disease: Ulnar deviation of the wrist
Ulnar deviation of the wrist 		14 0 5 0.14 0 0
CUI: C0231679
Disease: Ulnar deviation of the fingers
Ulnar deviation of the fingers 		31 0 7 0.14 0 0
CUI: C1446712
Disease: Overlapping fingers
Overlapping fingers 		27 0 6 0.13 0 0
CUI: C0265654
Disease: Tarsal Coalition
Tarsal Coalition 		22 0 5 0.12 0 0
CUI: C0685095
Disease: Biventricular congestive heart failure
Biventricular congestive heart failure 		3 0 3 0.12 0 0
CUI: C1836756
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder)
ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder) 		3 0 3 0.12 0 0
CUI: C1852597
Disease: Arthrogryposis, distal, type 2E
Arthrogryposis, distal, type 2E 		3 0 3 0.12 0 0
CUI: C1861238
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 10
ARTHROGRYPOSIS, DISTAL, TYPE 10 		3 0 3 0.12 0 0
CUI: C1862471
Disease: Arthrogryposis-like hand anomaly and sensorineural deafness
Arthrogryposis-like hand anomaly and sensorineural deafness 		3 0 3 0.12 0 0
CUI: C3554415
Disease: Distal arthrogryposis type 5D
Distal arthrogryposis type 5D 		3 0 3 0.12 0 0
CUI: C1862472
Disease: Oculomelic amyoplasia
Oculomelic amyoplasia 		4 0 3 0.11 0 0
CUI: C4272579
Disease: Autosomal Dominant Osteopetrosis
Autosomal Dominant Osteopetrosis 		14 0 4 0.11 0 0
CUI: C0265226
Disease: Hecht syndrome (disorder)
Hecht syndrome (disorder) 		5 0 3 0.11 0 0
CUI: C0003892
Disease: Neurogenic arthropathy
Neurogenic arthropathy 		7 0 3 1.0E-01 0 0
CUI: C4021735
Disease: Abnormality of the hip bone
Abnormality of the hip bone 		40 0 6 1.0E-01 0 0
CUI: C0268414
Disease: Hyperphosphatasemia with bone disease
Hyperphosphatasemia with bone disease 		8 0 3 9.7E-02 0 0
CUI: C0023222
Disease: Pain in lower limb
Pain in lower limb 		31 0 5 9.6E-02 0 0
CUI: C2749463
Disease: Aplasia/Hypoplasia of the radius
Aplasia/Hypoplasia of the radius 		45 0 6 9.2E-02 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy 		10 0 3 9.1E-02 0 0