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: C0032273
Disease: Pneumoconiosis
Pneumoconiosis 		33 0 14 0.42 0 0
CUI: C0041307
Disease: Tuberculosis, Bovine
Tuberculosis, Bovine 		1 0 1 7.1E-02 0 0
CUI: C0243025
Disease: Hantavirus Pulmonary Syndrome
Hantavirus Pulmonary Syndrome 		1 0 1 7.1E-02 0 0
CUI: C0343885
Disease: Chronic disseminated candidiasis
Chronic disseminated candidiasis 		1 0 1 7.1E-02 0 0
CUI: C0751631
Disease: Neurotoxoplasmosis
Neurotoxoplasmosis 		1 0 1 7.1E-02 0 0
CUI: C0796046
Disease: Gurrieri Sammito Bellussi syndrome
Gurrieri Sammito Bellussi syndrome 		1 0 1 7.1E-02 0 0
CUI: C1832827
Disease: DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8
DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8 		1 0 1 7.1E-02 0 0
CUI: C1838332
Disease: HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO
HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO 		1 0 1 7.1E-02 0 0
CUI: C1842149
Disease: Spondyloepiphyseal Dysplasia, Kimberley Type
Spondyloepiphyseal Dysplasia, Kimberley Type 		1 0 1 7.1E-02 0 0
CUI: C1856911
Disease: Ivory epiphyses
Ivory epiphyses 		1 0 1 7.1E-02 0 0
CUI: C1859478
Disease: Hypoplasia of proximal fibula
Hypoplasia of proximal fibula 		1 0 1 7.1E-02 0 0
CUI: C2748544
Disease: Spondyloepimetaphyseal Dysplasia, Aggrecan Type
Spondyloepimetaphyseal Dysplasia, Aggrecan Type 		1 0 1 7.1E-02 0 0
CUI: C2931854
Disease: Allergic Bronchopulmonary Mycosis
Allergic Bronchopulmonary Mycosis 		1 0 1 7.1E-02 0 0
CUI: C3152102
Disease: USH1D/F, CDH23/PCDH15, DIGENIC
USH1D/F, CDH23/PCDH15, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C3275872
Disease: USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC
USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC 		1 0 1 7.1E-02 0 0
CUI: C3281203
Disease: CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL 		1 0 1 7.1E-02 0 0
CUI: C3494623
Disease: Mild dementia
Mild dementia 		16 0 2 7.1E-02 0 0
CUI: C3539010
Disease: PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F 		1 0 1 7.1E-02 0 0
CUI: C3553869
Disease: ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6 		1 0 1 7.1E-02 0 0
CUI: C4015931
Disease: CARBONIC ANHYDRASE I, GUAM
CARBONIC ANHYDRASE I, GUAM 		1 0 1 7.1E-02 0 0
CUI: C4015932
Disease: CARBONIC ANHYDRASE I DEFICIENCY
CARBONIC ANHYDRASE I DEFICIENCY 		1 0 1 7.1E-02 0 0
CUI: C4021549
Disease: Euthyroid hyperthyroxinemia
Euthyroid hyperthyroxinemia 		1 0 1 7.1E-02 0 0
CUI: C0026103
Disease: Mikulicz Disease
Mikulicz Disease 		2 0 1 6.7E-02 0 0
CUI: C0032230
Disease: Pleural Rub
Pleural Rub 		2 0 1 6.7E-02 0 0
CUI: C0035234
Disease: Respiratory Sounds
Respiratory Sounds 		2 0 1 6.7E-02 0 0