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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia
0 11 0 0 2 1.0E-01
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 5.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 9.1E-02
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency
0 1 0 0 1 9.1E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 9.1E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 5.9E-02
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
0 123 0 0 1 7.5E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 9.1E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 2 0.18
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 8.3E-02
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated
0 2 0 0 1 8.3E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
0 2 0 0 1 8.3E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 9.1E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 7.7E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1
0 10 0 0 1 5.0E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 9.1E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 8.3E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 0.17
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 8.8E-03 0 0
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis
1 0 1 8.8E-03 0 0
CUI: C0006264
Disease: Bronchial Neoplasms
Bronchial Neoplasms
1 0 1 8.8E-03 0 0
CUI: C0006386
Disease: Bunion
Bunion
1 0 1 8.8E-03 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden
1 0 1 8.8E-03 0 0
CUI: C0011871
Disease: Diabetic peripheral angiopathy
Diabetic peripheral angiopathy
1 0 1 8.8E-03 0 0
CUI: C0013426
Disease: Dystrophy of vulva
Dystrophy of vulva
1 0 1 8.8E-03 0 0