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: C1852502
Disease: CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT 		45 0 10 8.3E-02 0 0
CUI: C2827469
Disease: Coronary Microvascular Disease
Coronary Microvascular Disease 		45 0 10 8.3E-02 0 0
CUI: C0011119
Disease: Decompression Sickness
Decompression Sickness 		98 0 14 8.2E-02 0 0
CUI: C0005398
Disease: Cholestasis, Extrahepatic
Cholestasis, Extrahepatic 		87 0 13 8.1E-02 0 0
CUI: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary 		115 0 15 8.1E-02 0 0
CUI: C0080032
Disease: Pleural Effusion, Malignant
Pleural Effusion, Malignant 		119 0 15 7.9E-02 0 0
CUI: C1370889
Disease: Liposarcoma, well differentiated
Liposarcoma, well differentiated 		54 0 10 7.7E-02 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 9 7.6E-02 0 0
CUI: C0027126
Disease: Myotonic Dystrophy
Myotonic Dystrophy 		155 0 17 7.6E-02 0 0
CUI: C0234958
Disease: Muscle degeneration
Muscle degeneration 		70 0 11 7.6E-02 0 0
CUI: C0234233
Disease: Sore to touch
Sore to touch 		56 0 10 7.6E-02 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 14 7.5E-02 0 0
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia 		30 0 8 7.4E-02 0 0
CUI: C1834674
Disease: BETHLEM MYOPATHY 1
BETHLEM MYOPATHY 1 		17 0 7 7.3E-02 0 0
CUI: C2347126
Disease: Microscopic Polyarteritis
Microscopic Polyarteritis 		77 0 11 7.2E-02 0 0
CUI: C1869123
Disease: Limb-girdle muscular dystrophy type 2A
Limb-girdle muscular dystrophy type 2A 		18 0 7 7.2E-02 0 0
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis 		35 0 8 7.1E-02 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 9 7.0E-02 0 0
CUI: C1861922
Disease: CAMPOMELIC DYSPLASIA
CAMPOMELIC DYSPLASIA 		68 0 10 6.9E-02 0 0
CUI: C4554215
Disease: Duchenne or Becker muscular dystrophy
Duchenne or Becker muscular dystrophy 		7 0 6 6.9E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		241 0 21 6.9E-02 0 0
CUI: C1851585
Disease: MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA
MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA 		119 0 13 6.8E-02 0 0
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition 		72 0 10 6.8E-02 0 0
CUI: C0451641
Disease: Urolithiasis
Urolithiasis 		72 0 10 6.8E-02 0 0
CUI: C0030552
Disease: Paresis
Paresis 		216 0 19 6.7E-02 0 0