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: C0278252
Disease: Prognosis bad
Prognosis bad
0 2 0 0 1 1.0E-02
WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1
0 1 0 0 1 1.0E-02
CUI: C2697788
Disease: Interleukin 8 Measurement
Interleukin 8 Measurement
0 5 0 0 1 1.0E-02
DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE
0 2 0 0 1 1.0E-02
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 1 6.0E-04 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 1 6.0E-04 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function
59 0 1 6.0E-04 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
55 0 1 6.1E-04 0 0
CUI: C0406208
Disease: Suntan
Suntan
53 0 1 6.1E-04 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs
51 0 1 6.1E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 1 6.1E-04 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb
42 0 1 6.1E-04 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block
39 0 1 6.1E-04 0 0
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
39 0 1 6.1E-04 0 0
CUI: C1844548
Disease: Hypoplastic finger
Hypoplastic finger
39 0 1 6.1E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 1 6.1E-04 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia
39 0 1 6.1E-04 0 0
CUI: C0239594
Disease: Short finger
Short finger
37 0 1 6.1E-04 0 0
CUI: C0007384
Disease: Cataplexy
Cataplexy
36 0 1 6.1E-04 0 0
CUI: C0598275
Disease: Diffuse cerebral atrophy
Diffuse cerebral atrophy
34 0 1 6.1E-04 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
32 0 1 6.1E-04 0 0
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination
32 0 1 6.1E-04 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness
31 0 1 6.1E-04 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome
31 0 1 6.1E-04 0 0
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc
31 0 1 6.1E-04 0 0