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 0.20 0 0
CUI: C0342826
Disease: 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency 		1 0 1 0.20 0 0
CUI: C0423729
Disease: Chest pain on breathing
Chest pain on breathing 		1 0 1 0.20 0 0
CUI: C1096121
Disease: Skeleton dysplasia
Skeleton dysplasia 		1 0 1 0.20 0 0
CUI: C1112616
Disease: Loss of proprioception
Loss of proprioception 		1 0 1 0.20 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 0.20 0 0
CUI: C2750413
Disease: Cap Myopathy, Tpm2-Related
Cap Myopathy, Tpm2-Related 		1 0 1 0.20 0 0
CUI: C2931649
Disease: Larsen syndrome, recessive type
Larsen syndrome, recessive type 		1 0 1 0.20 0 0
CUI: C3807907
Disease: CAP MYOPATHY 2
CAP MYOPATHY 2 		1 0 1 0.20 0 0
CUI: C4025044
Disease: Fixed elbow flexion
Fixed elbow flexion 		1 0 1 0.20 0 0
CUI: C4310692
Disease: ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH 		1 0 1 0.20 0 0
CUI: C0009701
Disease: Congenital dislocation
Congenital dislocation 		2 0 1 0.17 0 0
CUI: C0232066
Disease: Induced apnea
Induced apnea 		2 0 1 0.17 0 0
CUI: C0238045
Disease: Carotid-Cavernous Sinus Fistula
Carotid-Cavernous Sinus Fistula 		2 0 1 0.17 0 0
CUI: C1265768
Disease: Calcified aneurysm
Calcified aneurysm 		2 0 1 0.17 0 0
CUI: C1833326
Disease: Generalized bone demineralization
Generalized bone demineralization 		2 0 1 0.17 0 0
CUI: C1835573
Disease: Multiple carpal ossification centers
Multiple carpal ossification centers 		2 0 1 0.17 0 0
CUI: C1837073
Disease: Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy
Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 		2 0 1 0.17 0 0
CUI: C1850656
Disease: Firm muscles
Firm muscles 		2 0 1 0.17 0 0
CUI: C1854380
Disease: NEMALINE MYOPATHY 5
NEMALINE MYOPATHY 5 		2 0 1 0.17 0 0
CUI: C1855353
Disease: Fixed facial expression
Fixed facial expression 		2 0 1 0.17 0 0
CUI: C1868737
Disease: Vertebral artery hypoplasia
Vertebral artery hypoplasia 		2 0 1 0.17 0 0
CUI: C3275799
Disease: Spondylolisthesis at L5-S1
Spondylolisthesis at L5-S1 		2 0 1 0.17 0 0
CUI: C3278429
Disease: Bilateral elbow dislocations
Bilateral elbow dislocations 		2 0 1 0.17 0 0
CUI: C3898139
Disease: New or Worsening Symptom
New or Worsening Symptom 		2 0 1 0.17 0 0