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 1.6E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.8E-02
CUI: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric
0 4 0 0 1 1.7E-02
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
0 31 0 0 3 3.6E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 1.8E-02
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma
0 4 0 0 3 5.3E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
0 2 0 0 1 1.8E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.8E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 1.7E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1
0 10 0 0 1 1.5E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.8E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 1.8E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 1.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 3.5E-02
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
325 0 1 2.4E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
319 0 1 2.4E-03 0 0
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
308 0 1 2.5E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
269 0 1 2.8E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 0 1 2.8E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 1 2.8E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 1 2.9E-03 0 0
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
248 0 1 2.9E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.0E-03 0 0
CUI: C0085636
Disease: Photophobia
Photophobia
227 0 1 3.1E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 0 1 3.1E-03 0 0