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: C0013170
Disease: Drug habituation
Drug habituation
0 19 0 0 1 2.4E-02
CUI: C0015456
Disease: Facial Dermatoses
Facial Dermatoses
1 0 1 8.3E-02 0 0
CUI: C0343097
Disease: Nodular Elastoidosis
Nodular Elastoidosis
1 0 1 8.3E-02 0 0
CUI: C0345286
Disease: Abnormal liver lobulation
Abnormal liver lobulation
1 0 1 8.3E-02 0 0
CUI: C1842691
Disease: Diaphanospondylodysostosis
Diaphanospondylodysostosis
1 0 1 8.3E-02 0 0
CUI: C1842695
Disease: Absent in utero rib ossification
Absent in utero rib ossification
1 0 1 8.3E-02 0 0
Absent in utero ossification of vertebral bodies
1 0 1 8.3E-02 0 0
CUI: C2675562
Disease: Unossified sacrum
Unossified sacrum
1 0 1 8.3E-02 0 0
MACULAR DEGENERATION, AGE-RELATED, 15
1 0 1 8.3E-02 0 0
CUI: C4021093
Disease: Decreased serum complement C9
Decreased serum complement C9
1 0 1 8.3E-02 0 0
DRUG METABOLISM, ALTERED, CES1-RELATED
1 0 1 8.3E-02 0 0
CUI: C0015704
Disease: Favre-Racouchot Syndrome
Favre-Racouchot Syndrome
2 0 1 7.7E-02 0 0
CUI: C0428209
Disease: Leucine measurement
Leucine measurement
2 0 1 7.7E-02 0 0
CUI: C0751137
Disease: Craniofacial Pain
Craniofacial Pain
2 0 1 7.7E-02 0 0
Congenital Cataracts, Facial Dysmorphism, And Neuropathy
2 0 1 7.7E-02 0 0
CUI: C2675557
Disease: Lumbosacral meningocele
Lumbosacral meningocele
2 0 1 7.7E-02 0 0
CUI: C2675558
Disease: Nephroblastomatosis
Nephroblastomatosis
2 0 1 7.7E-02 0 0
CUI: C3151189
Disease: C9 Deficiency
C9 Deficiency
2 0 1 7.7E-02 0 0
CUI: C0008384
Disease: Cholesterol Ester Storage Disease
Cholesterol Ester Storage Disease
3 0 1 7.1E-02 0 0
Meningitis, Meningococcal, Serogroup A
3 0 1 7.1E-02 0 0
Meningitis, Meningococcal, Serogroup B
3 0 1 7.1E-02 0 0
Meningitis, Meningococcal, Serogroup C
3 0 1 7.1E-02 0 0
Meningitis, Meningococcal, Serogroup Y
3 0 1 7.1E-02 0 0
Meningitis, Meningococcal, Serogroup W-135
3 0 1 7.1E-02 0 0
CUI: C1866130
Disease: Rhombencephalosynapsis
Rhombencephalosynapsis
4 0 1 6.7E-02 0 0