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: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency
0 11 0 0 1 9.1E-02
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0 80 0 0 1 1.3E-02
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome
0 163 0 0 1 6.1E-03
CUI: C1843367
Disease: Poor school performance
Poor school performance
0 411 0 0 1 2.4E-03
CUI: C1859846
Disease: Childhood-onset truncal obesity
Childhood-onset truncal obesity
0 4 0 0 1 0.25
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder)
0 65 0 0 1 1.5E-02
CUI: C3808410
Disease: Gastrointestinal malrotation
Gastrointestinal malrotation
0 2 0 0 1 0.50
CUI: C4021330
Disease: Curved toe phalanx
Curved toe phalanx
0 1 0 0 1 1.00
CUI: C4022906
Disease: Delayed social development
Delayed social development
0 1 0 0 1 1.00
CUI: C0022492
Disease: Kandinsky Syndrome
Kandinsky Syndrome
1 0 1 5.3E-02 0 0
Ventricular Outflow Obstruction, Left
1 0 1 5.3E-02 0 0
Organic Brain Syndrome, Nonpsychotic
1 0 1 5.3E-02 0 0
CUI: C0029230
Disease: Organic Mental Disorders, Psychotic
Organic Mental Disorders, Psychotic
1 0 1 5.3E-02 0 0
CUI: C0033943
Disease: Psychoses, Traumatic
Psychoses, Traumatic
1 0 1 5.3E-02 0 0
Ventricular Outflow Obstruction, Right
1 0 1 5.3E-02 0 0
CUI: C0042512
Disease: Ventricular Outflow Obstruction
Ventricular Outflow Obstruction
1 0 1 5.3E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria
1 0 1 5.3E-02 0 0
CUI: C0154870
Disease: Focal chorioretinitis
Focal chorioretinitis
1 0 1 5.3E-02 0 0
Syndrome of infant of diabetic mother
1 0 1 5.3E-02 0 0
CUI: C0270730
Disease: MPTP Poisoning
MPTP Poisoning
1 0 1 5.3E-02 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia
1 0 1 5.3E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia
1 0 1 5.3E-02 0 0
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy
1 0 1 5.3E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness
1 0 1 5.3E-02 0 0
CUI: C0344297
Disease: Choroidal sclerosis
Choroidal sclerosis
1 0 1 5.3E-02 0 0