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 2.7E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 3.4E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 3.4E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 3.4E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 3.2E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.4E-02
ACQUIRED IMMUNODEFICIENCY SYNDROME, DELAYED PROGRESSION TO
0 1 0 0 1 3.4E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 6.7E-02
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement
169 0 1 1.8E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 1.8E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 1 1.8E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea
129 0 1 1.9E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause
129 0 1 1.9E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
104 0 1 2.0E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 1 2.0E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 1 2.0E-03 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
100 0 1 2.0E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation
98 0 1 2.0E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 1 2.0E-03 0 0
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
88 0 1 2.1E-03 0 0
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
88 0 1 2.1E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 1 2.1E-03 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
83 0 1 2.1E-03 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
83 0 1 2.1E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement
82 0 1 2.1E-03 0 0