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: C0001948
Disease: Alcohol consumption
Alcohol consumption 		210 0 1 4.8E-03 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		109 0 1 9.2E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 1.1E-02 0 0
CUI: C0022679
Disease: Cystic kidney
Cystic kidney 		89 0 1 1.1E-02 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 6.0E-03 0 0
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		714 0 1 1.4E-03 0 0
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood 		33 0 1 3.0E-02 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		227 0 1 4.4E-03 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 1 2.3E-02 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 1 3.8E-02 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		338 0 1 3.0E-03 0 0
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		139 0 1 7.2E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		610 0 1 1.6E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 6.8E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 1.8E-02 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 1 5.0E-02 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		20 0 1 5.0E-02 0 0
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		507 0 1 2.0E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		146 0 1 6.8E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 1.1E-02 0 0
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		139 0 1 7.2E-03 0 0
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		843 0 1 1.2E-03 0 0
CUI: C1836946
Disease: Peripheral Cone Dystrophy
Peripheral Cone Dystrophy 		1 0 1 1.00 0 0
CUI: C1859308
Disease: PREMATURE CENTROMERE DIVISION
PREMATURE CENTROMERE DIVISION 		66 0 1 1.5E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 4.7E-03 0 0