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 5.2E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 5.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 5.3E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia
0 1 0 0 1 5.4E-03
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 5.2E-03
HYPERPARATHYROIDISM, NEONATAL SEVERE
0 14 0 0 1 5.1E-03
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated
0 2 0 0 1 5.4E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 5.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 5.4E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 5.4E-03
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM
0 14 0 0 2 1.0E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 1.1E-02
CUI: C0000729
Disease: Abdominal Cramps
Abdominal Cramps
1 0 1 2.1E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 2.1E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 2.1E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 2.1E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 2.0E-03 0 0
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma
11 0 1 2.1E-03 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil
2 0 1 2.1E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 1 2.1E-03 0 0
CUI: C0001630
Disease: Adrenal Rest Tumor
Adrenal Rest Tumor
2 0 1 2.1E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia
17 0 1 2.1E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia
3 0 1 2.1E-03 0 0
CUI: C0001828
Disease: Agricultural Workers' Diseases
Agricultural Workers' Diseases
1 0 1 2.1E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 1.9E-03 0 0