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 5.6E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.0E-01
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder
0 1 0 0 1 1.0E-01
CUI: C0206042
Disease: Fatal Familial Insomnia
Fatal Familial Insomnia
0 16 0 0 1 4.0E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 1 7.1E-02
CUI: C1405458
Disease: Language Problems
Language Problems
0 2 0 0 1 9.1E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 5.6E-02
CUI: C1864112
Disease: HUNTINGTON DISEASE-LIKE 1
HUNTINGTON DISEASE-LIKE 1
0 4 0 0 1 7.7E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
0 3 0 0 1 8.3E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.0E-01
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.0E-01
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 9.1E-02
CUI: C4275003
Disease: Familial Creutzfeldt-Jakob
Familial Creutzfeldt-Jakob
0 1 0 0 1 1.0E-01
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1
0 36 0 0 1 2.2E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 8.3E-02
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 5.7E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 5.4E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 5.8E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis
9 0 1 5.8E-03 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma
8 0 1 5.9E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia
17 0 1 5.6E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia
3 0 1 6.1E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis
13 0 1 5.7E-03 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness
10 0 1 5.8E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta
61 0 1 4.5E-03 0 0