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 7.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 7.9E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 7.9E-03
CUI: C0334328
Disease: Microfollicular adenoma
Microfollicular adenoma
0 1 0 0 1 7.9E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 7.9E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 7.9E-03
CUI: C0814144
Disease: endocrine system cancer
endocrine system cancer
0 1 0 0 1 7.9E-03
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0 478 0 0 2 3.3E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 7.9E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 7.8E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 7.9E-03
CUI: C4310620
Disease: Yao syndrome
Yao syndrome
0 3 0 0 1 7.8E-03
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
98 0 1 8.8E-04 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology
86 0 1 8.9E-04 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 8.9E-04 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance
76 0 1 8.9E-04 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb
74 0 1 9.0E-04 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly
62 0 1 9.1E-04 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 1 9.1E-04 0 0
Fatigable weakness of respiratory muscles
60 0 1 9.1E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 1 9.1E-04 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function
59 0 1 9.1E-04 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 1 9.1E-04 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum
57 0 1 9.1E-04 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 0 1 9.1E-04 0 0