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: C0220726
Disease: Diastrophic dysplasia
Diastrophic dysplasia 		56 63 33 0.41 12 0.17
CUI: C0677659
Disease: Gastro-esophageal reflux disease with esophagitis
Gastro-esophageal reflux disease with esophagitis 		71 0 9 7.6E-02 0 0
CUI: C0079298
Disease: Epidermolysis Bullosa Simplex
Epidermolysis Bullosa Simplex 		30 0 6 7.4E-02 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 7 7.4E-02 0 0
CUI: C1301700
Disease: Cardiovascular morbidity
Cardiovascular morbidity 		75 0 9 7.3E-02 0 0
CUI: C2733158
Disease: Cerebral Small Vessel Diseases
Cerebral Small Vessel Diseases 		62 0 8 7.2E-02 0 0
CUI: C0023643
Disease: Lichen disease
Lichen disease 		33 0 6 7.1E-02 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder) 		20 0 5 6.9E-02 0 0
CUI: C0014869
Disease: Peptic Esophagitis
Peptic Esophagitis 		85 0 9 6.8E-02 0 0
CUI: C0860197
Disease: Advanced chronic liver disease
Advanced chronic liver disease 		7 0 4 6.7E-02 0 0
CUI: C4324685
Disease: Hypertensive end-organ damage
Hypertensive end-organ damage 		9 0 4 6.5E-02 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		92 0 9 6.4E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 8 6.4E-02 0 0
CUI: C0003969
Disease: Ascorbic Acid Deficiency
Ascorbic Acid Deficiency 		10 0 4 6.3E-02 0 0
CUI: C4287997
Disease: WHO Grade III Glioma
WHO Grade III Glioma 		10 0 4 6.3E-02 0 0
CUI: C1739395
Disease: Takotsubo Cardiomyopathy
Takotsubo Cardiomyopathy 		44 0 6 6.3E-02 0 0
CUI: C0259749
Disease: Autonomic neuropathy
Autonomic neuropathy 		29 0 5 6.2E-02 0 0
CUI: C3826128
Disease: Infection in children
Infection in children 		29 0 5 6.2E-02 0 0
CUI: C0270500
Disease: Coprophilia (disorder)
Coprophilia (disorder) 		12 0 4 6.2E-02 0 0
CUI: C0004775
Disease: Bartter Disease
Bartter Disease 		47 0 6 6.1E-02 0 0
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda 		30 0 5 6.1E-02 0 0
CUI: C0948268
Disease: Hemodynamic instability
Hemodynamic instability 		15 0 4 5.9E-02 0 0
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension 		52 0 6 5.8E-02 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 5 5.7E-02 0 0
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss 		72 0 7 5.7E-02 0 0