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: C0014493
Disease: Epidemic keratoconjunctivitis
Epidemic keratoconjunctivitis 		6 0 1 0.17 0 0
CUI: C0031538
Disease: Phimosis
Phimosis 		6 0 1 0.17 0 0
CUI: C0344893
Disease: Right ventricular dilatation
Right ventricular dilatation 		6 0 1 0.17 0 0
CUI: C1879286
Disease: Hereditary bundle branch system defect
Hereditary bundle branch system defect 		7 0 1 0.14 0 0
CUI: C1969236
Disease: Mitten deformity
Mitten deformity 		7 0 1 0.14 0 0
CUI: C3150852
Disease: EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION 		7 0 1 0.14 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 9.1E-02 0 0
CUI: C0853945
Disease: Oral mucosal blisters
Oral mucosal blisters 		12 0 1 8.3E-02 0 0
CUI: C0151970
Disease: Ulcer of esophagus
Ulcer of esophagus 		13 0 1 7.7E-02 0 0
CUI: C0017572
Disease: Gingival Recession
Gingival Recession 		14 0 1 7.1E-02 0 0
CUI: C0241984
Disease: Honeycomb lung
Honeycomb lung 		14 0 1 7.1E-02 0 0
CUI: C4476639
Disease: Ground-glass opacification on pulmonary HRCT
Ground-glass opacification on pulmonary HRCT 		14 0 1 7.1E-02 0 0
CUI: C4476748
Disease: Reticular pattern on pulmonary HRCT
Reticular pattern on pulmonary HRCT 		14 0 1 7.1E-02 0 0
CUI: C2063326
Disease: Right ventricular cardiomyopathy
Right ventricular cardiomyopathy 		15 0 1 6.7E-02 0 0
CUI: C0018500
Disease: Hair Diseases
Hair Diseases 		17 0 1 5.9E-02 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change 		18 0 1 5.6E-02 0 0
CUI: C0263505
Disease: Alopecia universalis
Alopecia universalis 		19 0 1 5.3E-02 0 0
CUI: C0334013
Disease: Phrynoderma
Phrynoderma 		19 0 1 5.3E-02 0 0
CUI: C0343073
Disease: Wooly hair
Wooly hair 		19 0 1 5.3E-02 0 0
CUI: C2931783
Disease: Amelogenesis imperfecta nephrocalcinosis
Amelogenesis imperfecta nephrocalcinosis 		19 0 1 5.3E-02 0 0
CUI: C4721530
Disease: Congenital hypotrichia
Congenital hypotrichia 		19 0 1 5.3E-02 0 0
CUI: C0079153
Disease: Hyperkeratosis, Epidermolytic
Hyperkeratosis, Epidermolytic 		20 0 1 5.0E-02 0 0
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1 		20 0 1 5.0E-02 0 0
CUI: C4721508
Disease: Hamman-Rich Disease
Hamman-Rich Disease 		20 0 1 5.0E-02 0 0
CUI: C0027443
Disease: Natal Teeth
Natal Teeth 		22 0 1 4.5E-02 0 0