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: C1852597
Disease: Arthrogryposis, distal, type 2E
Arthrogryposis, distal, type 2E 		3 0 3 1.00 0 0
CUI: C1861238
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 10
ARTHROGRYPOSIS, DISTAL, TYPE 10 		3 0 3 1.00 0 0
CUI: C1862471
Disease: Arthrogryposis-like hand anomaly and sensorineural deafness
Arthrogryposis-like hand anomaly and sensorineural deafness 		3 0 3 1.00 0 0
CUI: C3554415
Disease: Distal arthrogryposis type 5D
Distal arthrogryposis type 5D 		3 0 3 1.00 0 0
CUI: C1862472
Disease: Oculomelic amyoplasia
Oculomelic amyoplasia 		4 0 3 0.75 0 0
CUI: C3280526
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1B
ARTHROGRYPOSIS, DISTAL, TYPE 1B 		4 0 3 0.75 0 0
CUI: C0265226
Disease: Hecht syndrome (disorder)
Hecht syndrome (disorder) 		5 0 3 0.60 0 0
CUI: C0220662
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1
ARTHROGRYPOSIS, DISTAL, TYPE 1 		9 0 3 0.33 0 0
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 0.33 0 0
CUI: C4476577
Disease: Incomitant strabismus
Incomitant strabismus 		1 0 1 0.33 0 0
CUI: C0857276
Disease: Patellar subluxation
Patellar subluxation 		2 0 1 0.25 0 0
CUI: C1970777
Disease: Abnormally folded helix
Abnormally folded helix 		2 0 1 0.25 0 0
CUI: C3805450
Disease: Calf muscle hypoplasia
Calf muscle hypoplasia 		2 0 1 0.25 0 0
CUI: C0220666
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA 		15 0 3 0.20 0 0
CUI: C1862479
Disease: Absent phalangeal crease
Absent phalangeal crease 		3 0 1 0.20 0 0
CUI: C4016054
Disease: Neonatal Marfan syndrome
Neonatal Marfan syndrome 		3 0 1 0.20 0 0
CUI: C0277005
Disease: Opisthorchis viverrini Infection
Opisthorchis viverrini Infection 		4 0 1 0.17 0 0
CUI: C0409354
Disease: Flexion contracture of hip
Flexion contracture of hip 		4 0 1 0.17 0 0
CUI: C4025596
Disease: Abnormality of connective tissue
Abnormality of connective tissue 		4 0 1 0.17 0 0
CUI: C1393871
Disease: Congenital finger flexion contractures
Congenital finger flexion contractures 		5 0 1 0.14 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		22 0 3 0.14 0 0
CUI: C1852085
Disease: Digitotalar Dysmorphism
Digitotalar Dysmorphism 		6 0 1 0.12 0 0
CUI: C1866487
Disease: Prominent nasolabial fold
Prominent nasolabial fold 		6 0 1 0.12 0 0
CUI: C4015286
Disease: MACULAR DEGENERATION, EARLY-ONSET
MACULAR DEGENERATION, EARLY-ONSET 		6 0 1 0.12 0 0
CUI: C4024166
Disease: Crumpled ear
Crumpled ear 		6 0 1 0.12 0 0