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: C0027643
Disease: Neoplasm Recurrence, Local
Neoplasm Recurrence, Local
39 0 1 2.6E-02 0 0
CUI: C0240602
Disease: opioid use
opioid use
39 0 1 2.6E-02 0 0
CUI: C1298820
Disease: Aneurysm of aortic root
Aneurysm of aortic root
39 0 1 2.6E-02 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly
40 0 1 2.5E-02 0 0
CUI: C0750929
Disease: Arnold-Chiari Malformation, Type I
Arnold-Chiari Malformation, Type I
41 0 1 2.4E-02 0 0
CUI: C1839797
Disease: Deep philtrum
Deep philtrum
42 0 1 2.4E-02 0 0
CUI: C0026552
Disease: Morphine Dependence
Morphine Dependence
44 0 1 2.3E-02 0 0
CUI: C0678202
Disease: Regional enteritis
Regional enteritis
46 0 1 2.2E-02 0 0
CUI: C1739405
Disease: CML progression
CML progression
47 0 1 2.1E-02 0 0
CUI: C3714542
Disease: Lymphoma, Diffuse
Lymphoma, Diffuse
49 0 1 2.0E-02 0 0
CUI: C0424139
Disease: Anxiety and fear
Anxiety and fear
51 0 1 2.0E-02 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation
53 0 1 1.9E-02 0 0
CUI: C0949272
Disease: IIeocolitis
IIeocolitis
53 0 1 1.9E-02 0 0
CUI: C0267380
Disease: Crohn's disease of the ileum
Crohn's disease of the ileum
55 0 1 1.8E-02 0 0
CUI: C0265202
Disease: Seckel syndrome
Seckel syndrome
56 0 1 1.8E-02 0 0
CUI: C1836195
Disease: Short toe
Short toe
56 0 1 1.8E-02 0 0
CUI: C0410000
Disease: Overlap syndrome
Overlap syndrome
57 0 1 1.8E-02 0 0
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve
59 0 1 1.7E-02 0 0
CUI: C0040961
Disease: Tricuspid Valve Insufficiency
Tricuspid Valve Insufficiency
60 0 1 1.7E-02 0 0
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels
61 0 1 1.6E-02 0 0
CUI: C0596240
Disease: Cancer Pain
Cancer Pain
62 0 1 1.6E-02 0 0
Treatment related acute myeloid leukaemia
65 0 1 1.5E-02 0 0
CUI: C3496069
Disease: cocaine use
cocaine use
67 0 1 1.5E-02 0 0
CUI: C0206696
Disease: Carcinoma, Signet Ring Cell
Carcinoma, Signet Ring Cell
70 0 1 1.4E-02 0 0
CUI: C0279646
Disease: Childhood Acute Monocytic Leukemia
Childhood Acute Monocytic Leukemia
70 0 1 1.4E-02 0 0