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: C0270149
Disease: Perinatal respiratory distress
Perinatal respiratory distress 		1 0 1 1.00 0 0
CUI: C1112616
Disease: Loss of proprioception
Loss of proprioception 		1 0 1 1.00 0 0
CUI: C4310692
Disease: ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH 		1 0 1 1.00 0 0
CUI: C0232066
Disease: Induced apnea
Induced apnea 		2 0 1 0.50 0 0
CUI: C1850656
Disease: Firm muscles
Firm muscles 		2 0 1 0.50 0 0
CUI: C1855353
Disease: Fixed facial expression
Fixed facial expression 		2 0 1 0.50 0 0
CUI: C3275799
Disease: Spondylolisthesis at L5-S1
Spondylolisthesis at L5-S1 		2 0 1 0.50 0 0
CUI: C1862474
Disease: Decreased facial expression
Decreased facial expression 		3 0 1 0.33 0 0
CUI: C1862479
Disease: Absent phalangeal crease
Absent phalangeal crease 		3 0 1 0.33 0 0
CUI: C4021251
Disease: Dysplasia of the femoral head
Dysplasia of the femoral head 		3 0 1 0.33 0 0
CUI: C0575803
Disease: Radial deviation of hand
Radial deviation of hand 		4 0 1 0.25 0 0
CUI: C1862472
Disease: Oculomelic amyoplasia
Oculomelic amyoplasia 		4 0 1 0.25 0 0
CUI: C0036686
Disease: Gram positive sepsis
Gram positive sepsis 		5 0 1 0.20 0 0
CUI: C0410740
Disease: Acquired deformity of finger
Acquired deformity of finger 		5 0 1 0.20 0 0
CUI: C1393871
Disease: Congenital finger flexion contractures
Congenital finger flexion contractures 		5 0 1 0.20 0 0
CUI: C1836589
Disease: Decreased hip abduction
Decreased hip abduction 		5 0 1 0.20 0 0
CUI: C1851313
Disease: Limited shoulder movement
Limited shoulder movement 		5 0 1 0.20 0 0
CUI: C1855350
Disease: Inferior vermis hypoplasia
Inferior vermis hypoplasia 		5 0 1 0.20 0 0
CUI: C1862481
Disease: Limited wrist extension
Limited wrist extension 		5 0 1 0.20 0 0
CUI: C1857483
Disease: Decreased palmar creases
Decreased palmar creases 		6 0 1 0.17 0 0
CUI: C4025712
Disease: Abnormality of the cerebellar vermis
Abnormality of the cerebellar vermis 		6 0 1 0.17 0 0
CUI: C0796033
Disease: MARDEN-WALKER SYNDROME
MARDEN-WALKER SYNDROME 		8 0 1 0.12 0 0
CUI: C0038018
Disease: Spondylolysis
Spondylolysis 		9 0 1 0.11 0 0
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		9 0 1 0.11 0 0
CUI: C4021262
Disease: Absent palmar crease
Absent palmar crease 		9 0 1 0.11 0 0