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: C1844690
Disease: Limited knee extension
Limited knee extension
11 0 2 8.7E-02 0 0
CUI: C2364016
Disease: Systemic sclerosis [scleroderma]
Systemic sclerosis [scleroderma]
11 0 2 8.7E-02 0 0
CUI: C0393574
Disease: Huntington Disease, Late Onset
Huntington Disease, Late Onset
12 0 2 8.3E-02 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion
12 0 2 8.3E-02 0 0
Akinetic-Rigid Variant of Huntington Disease
12 0 2 8.3E-02 0 0
CUI: C0751208
Disease: Juvenile Huntington Disease
Juvenile Huntington Disease
12 0 2 8.3E-02 0 0
CUI: C2936476
Disease: Chronic Liver Failure
Chronic Liver Failure
25 0 3 8.3E-02 0 0
CUI: C0030662
Disease: Gambling, Pathological
Gambling, Pathological
26 0 3 8.1E-02 0 0
CUI: C4046029
Disease: Mental Disorders, Severe
Mental Disorders, Severe
26 0 3 8.1E-02 0 0
CUI: C0003477
Disease: Separation Anxiety Disorder
Separation Anxiety Disorder
13 0 2 8.0E-02 0 0
CUI: C0149875
Disease: Primary dysmenorrhea
Primary dysmenorrhea
13 0 2 8.0E-02 0 0
CUI: C0149886
Disease: Seizure, Febrile, Simple
Seizure, Febrile, Simple
13 0 2 8.0E-02 0 0
CUI: C0338596
Disease: Spastic cerebral palsy
Spastic cerebral palsy
13 0 2 8.0E-02 0 0
Neuropathy due to human immunodeficiency virus
13 0 2 8.0E-02 0 0
CUI: C0857177
Disease: Arthritic pain
Arthritic pain
13 0 2 8.0E-02 0 0
Generalized Epilepsy with Febrile Seizures Plus
13 0 2 8.0E-02 0 0
CUI: C3892044
Disease: Oligoarticular Arthritis
Oligoarticular Arthritis
13 0 2 8.0E-02 0 0
CUI: C0024517
Disease: Major depression, single episode
Major depression, single episode
42 0 4 7.7E-02 0 0
CUI: C0158026
Disease: Monoarthritis
Monoarthritis
14 0 2 7.7E-02 0 0
CUI: C0158458
Disease: Acquired hallux valgus
Acquired hallux valgus
14 0 2 7.7E-02 0 0
CUI: C0265656
Disease: Congenital hallux valgus
Congenital hallux valgus
14 0 2 7.7E-02 0 0
CUI: C0858853
Disease: Impulsive aggression
Impulsive aggression
14 0 2 7.7E-02 0 0
Generalized cerebral atrophy/hypoplasia
14 0 2 7.7E-02 0 0
Mesial temporal lobe epilepsy with hippocampal sclerosis
14 0 2 7.7E-02 0 0
CUI: C0021308
Disease: Infarction
Infarction
15 0 2 7.4E-02 0 0