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: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis
1 0 1 3.0E-03 0 0
CUI: C0002831
Disease: Ancylostomiasis
Ancylostomiasis
1 0 1 3.0E-03 0 0
CUI: C0002897
Disease: Anemia, Splenic
Anemia, Splenic
1 0 1 3.0E-03 0 0
CUI: C0003708
Disease: Arachnoiditis
Arachnoiditis
1 0 1 3.0E-03 0 0
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders
1 0 1 3.0E-03 0 0
CUI: C0003944
Disease: As If Personality
As If Personality
1 0 1 3.0E-03 0 0
CUI: C0005424
Disease: Biliary Tract Diseases
Biliary Tract Diseases
1 0 1 3.0E-03 0 0
CUI: C0005723
Disease: Oral paracoccidioidomycosis
Oral paracoccidioidomycosis
1 0 1 3.0E-03 0 0
CUI: C0006015
Disease: Bordetella Infections
Bordetella Infections
1 0 1 3.0E-03 0 0
CUI: C0006264
Disease: Bronchial Neoplasms
Bronchial Neoplasms
1 0 1 3.0E-03 0 0
CUI: C0006386
Disease: Bunion
Bunion
1 0 1 3.0E-03 0 0
CUI: C0006915
Disease: Caplan Syndrome
Caplan Syndrome
1 0 1 3.0E-03 0 0