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 5.0E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 8.3E-02
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder
0 1 0 0 1 8.3E-02
CUI: C0206042
Disease: Fatal Familial Insomnia
Fatal Familial Insomnia
0 16 0 0 1 3.7E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 1 6.2E-02
CUI: C1405458
Disease: Language Problems
Language Problems
0 2 0 0 1 7.7E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 5.0E-02
CUI: C1864112
Disease: HUNTINGTON DISEASE-LIKE 1
HUNTINGTON DISEASE-LIKE 1
0 4 0 0 1 6.7E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
0 3 0 0 1 7.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 8.3E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 8.3E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 7.7E-02
CUI: C4275003
Disease: Familial Creutzfeldt-Jakob
Familial Creutzfeldt-Jakob
0 1 0 0 1 8.3E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 5.0E-02
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM
0 14 0 0 2 8.3E-02
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual
7 0 1 5.6E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 5.4E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 5.5E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 5.6E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 5.4E-03 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma
8 0 1 5.6E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 4 1 5.5E-03 1 6.7E-02
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 1 5.5E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia
17 0 1 5.3E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia
3 0 1 5.7E-03 0 0