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: C2825877
Disease: Interferon Gamma Measurement
Interferon Gamma Measurement
5 0 1 6.2E-02 0 0
CUI: C3808270
Disease: Acetabular spurs
Acetabular spurs
5 0 1 6.2E-02 0 0
Short rib-polydactyly syndrome, Beemer type
6 0 1 5.9E-02 0 0
CUI: C1845272
Disease: Prominent antihelix
Prominent antihelix
6 0 1 5.9E-02 0 0
Macular Degeneration, Age-Related, 1
6 0 1 5.9E-02 0 0
CUI: C4023170
Disease: Abnormal oral mucosa morphology
Abnormal oral mucosa morphology
6 0 1 5.9E-02 0 0
CUI: C0018672
Disease: Head Banging
Head Banging
7 0 1 5.6E-02 0 0
CUI: C0032176
Disease: Platelet aggregation
Platelet aggregation
7 0 1 5.6E-02 0 0
CUI: C0231779
Disease: Heel toe gait
Heel toe gait
7 0 1 5.6E-02 0 0
CUI: C0428321
Disease: Measurement of liver enzyme
Measurement of liver enzyme
7 0 1 5.6E-02 0 0
CUI: C1287351
Disease: Finding of liver enzyme levels
Finding of liver enzyme levels
7 0 1 5.6E-02 0 0
CUI: C4048548
Disease: Anti-Mullerian Hormone Measurement
Anti-Mullerian Hormone Measurement
7 0 1 5.6E-02 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle
48 0 3 5.3E-02 0 0
CUI: C1846433
Disease: Prominent sternum
Prominent sternum
8 0 1 5.3E-02 0 0
CUI: C1857002
Disease: Capitate-hamate fusion
Capitate-hamate fusion
8 0 1 5.3E-02 0 0
CUI: C4024965
Disease: Frontal cortical atrophy
Frontal cortical atrophy
8 0 1 5.3E-02 0 0
Congenital malformation of corpus callosum
9 0 1 5.0E-02 0 0
CUI: C4024912
Disease: Occipital myelomeningocele
Occipital myelomeningocele
9 0 1 5.0E-02 0 0
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
10 0 1 4.8E-02 0 0
CUI: C1856136
Disease: Conical incisor
Conical incisor
10 0 1 4.8E-02 0 0
CUI: C0013903
Disease: Ellis-Van Creveld Syndrome
Ellis-Van Creveld Syndrome
11 0 1 4.5E-02 0 0
Sex hormone binding globulin measurement
11 0 1 4.5E-02 0 0
CUI: C0392482
Disease: Common atrium
Common atrium
11 0 1 4.5E-02 0 0
CUI: C1518716
Disease: Ovarian gonadoblastoma
Ovarian gonadoblastoma
11 0 1 4.5E-02 0 0
CUI: C2748910
Disease: Rett Syndrome, Atypical
Rett Syndrome, Atypical
11 0 1 4.5E-02 0 0