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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 2.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 2.6E-02
CUI: C0340992
Disease: Cryoglobulinemic vasculitis
Cryoglobulinemic vasculitis
0 1 0 0 1 2.6E-02
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 2.6E-02
Hepatitis Virus-Related Hepatocellular Carcinoma
0 2 0 0 1 2.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 2.6E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 2.5E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1
0 10 0 0 1 2.1E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 2.6E-02
CUI: C4049395
Disease: Chronic hepatitis C genotype 2
Chronic hepatitis C genotype 2
0 1 0 0 1 2.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 5.1E-02
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 0 1 1.9E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
218 0 1 2.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 2.0E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement
169 0 1 2.2E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.2E-03 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders
167 0 1 2.2E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 1 2.2E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 2.2E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead
149 0 1 2.3E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 1 2.3E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial
142 0 1 2.3E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment
136 0 1 2.3E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.4E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay
130 0 1 2.4E-03 0 0