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: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition 		72 0 9 6.6E-02 0 0
CUI: C0451641
Disease: Urolithiasis
Urolithiasis 		72 0 9 6.6E-02 0 0
CUI: C2347126
Disease: Microscopic Polyarteritis
Microscopic Polyarteritis 		77 0 9 6.3E-02 0 0
CUI: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary 		115 0 11 6.2E-02 0 0
CUI: C0080032
Disease: Pleural Effusion, Malignant
Pleural Effusion, Malignant 		119 0 11 6.0E-02 0 0
CUI: C1851585
Disease: MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA
MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA 		119 0 11 6.0E-02 0 0
CUI: C0005398
Disease: Cholestasis, Extrahepatic
Cholestasis, Extrahepatic 		87 0 9 5.9E-02 0 0
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
MYOTONIC DYSTROPHY 1 		179 0 14 5.9E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		241 0 17 5.7E-02 0 0
CUI: C0005967
Disease: Bone neoplasms
Bone neoplasms 		151 0 12 5.6E-02 0 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 6 5.6E-02 0 0
CUI: C0005859
Disease: Bloom Syndrome
Bloom Syndrome 		155 0 12 5.5E-02 0 0
CUI: C0027126
Disease: Myotonic Dystrophy
Myotonic Dystrophy 		155 0 12 5.5E-02 0 0
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 317 5 5.4E-02 1 2.3E-03
CUI: C2745945
Disease: Juvenile-Onset Vitelliform Macular Dystrophy
Juvenile-Onset Vitelliform Macular Dystrophy 		4 0 4 5.4E-02 0 0
CUI: C4024817
Disease: Vitelliform-like macular lesions
Vitelliform-like macular lesions 		4 0 4 5.4E-02 0 0
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy 		24 0 5 5.4E-02 0 0
CUI: C0282193
Disease: Iron Overload
Iron Overload 		241 0 16 5.4E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 6 5.3E-02 0 0
CUI: C0019202
Disease: Hepatolenticular Degeneration
Hepatolenticular Degeneration 		146 0 11 5.3E-02 0 0
CUI: C3887875
Disease: Visual field defects
Visual field defects 		47 0 6 5.2E-02 0 0
CUI: C1720251
Disease: Retinal pigment epithelium atrophy
Retinal pigment epithelium atrophy 		7 0 4 5.2E-02 0 0
CUI: C2733564
Disease: Full thickness hole of macula lutea
Full thickness hole of macula lutea 		7 0 4 5.2E-02 0 0
CUI: C4021563
Disease: Retinal nonattachment
Retinal nonattachment 		7 0 4 5.2E-02 0 0
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina 		49 24 6 5.1E-02 5 3.6E-02