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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic
0 1 0 0 1 7.6E-03
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
0 31 0 0 3 1.9E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 1.5E-02
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement
0 51 0 0 1 5.5E-03
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement
0 51 0 0 1 5.5E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess
0 3 0 0 2 1.5E-02
Atrophia Maculosa Varioliformis Cutis, Familial
0 1 0 0 1 7.6E-03
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
0 1 0 0 1 7.6E-03
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
0 1 0 0 1 7.6E-03
CUI: C2242456
Disease: thyroid function
thyroid function
0 60 0 0 1 5.3E-03
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO
0 3 0 0 1 7.5E-03
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder
0 2 0 0 1 7.6E-03
progressive non-small cell lung cancer
0 1 0 0 1 7.6E-03
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 1.8E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 1 2.0E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control
162 0 1 2.0E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.0E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
148 0 1 2.1E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 1 2.1E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady
143 0 1 2.1E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia
142 0 1 2.1E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 1 2.1E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
131 0 1 2.2E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.2E-03 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios
129 0 1 2.2E-03 0 0