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: C1449862
Disease: Micronuclei, Genotoxicant-Induced
Micronuclei, Genotoxicant-Induced
26 0 26 1.00 0 0
CUI: C0028797
Disease: Occupational Diseases
Occupational Diseases
22 0 6 0.14 0 0
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
24 0 6 0.14 0 0
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
8 0 4 0.13 0 0
CUI: C1304119
Disease: Chronic stable plaque psoriasis
Chronic stable plaque psoriasis
5 0 3 0.11 0 0
CUI: C0376628
Disease: Chromosome Breakage
Chromosome Breakage
17 0 4 0.10 0 0
CUI: C1257806
Disease: Chromosomal Instability
Chromosomal Instability
8 0 3 9.7E-02 0 0
CUI: C4023759
Disease: Flat nasal alae
Flat nasal alae
8 0 3 9.7E-02 0 0
CUI: C0022593
Disease: Keratosis
Keratosis
43 0 6 9.5E-02 0 0
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
20 0 4 9.5E-02 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A
48 0 6 8.8E-02 0 0
CUI: C0153405
Disease: Malignant neoplasm of pharynx
Malignant neoplasm of pharynx
37 0 5 8.6E-02 0 0
Defective DNA repair after ultraviolet radiation damage
12 0 3 8.6E-02 0 0
CUI: C0016978
Disease: gallbladder neoplasm
gallbladder neoplasm
51 0 6 8.5E-02 0 0
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris
13 0 3 8.3E-02 0 0
CUI: C0333704
Disease: Chromosome Breaks
Chromosome Breaks
14 0 3 8.1E-02 0 0
Xeroderma Pigmentosum, Complementation Group D
70 0 7 7.9E-02 0 0
CUI: C0004403
Disease: Autosome Abnormalities
Autosome Abnormalities
16 0 3 7.7E-02 0 0
CUI: C0008625
Disease: Chromosome Aberrations
Chromosome Aberrations
16 0 3 7.7E-02 0 0
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda
30 0 4 7.7E-02 0 0
CUI: C0016689
Disease: Freckles
Freckles
45 0 5 7.6E-02 0 0
Fast acetylator due to N-acetyltransferase enzyme variant
17 0 3 7.5E-02 0 0
CUI: C0014390
Disease: Entropion
Entropion
18 0 3 7.3E-02 0 0
CUI: C0152233
Disease: Congenital ankyloblepharon
Congenital ankyloblepharon
18 0 3 7.3E-02 0 0
CUI: C0339182
Disease: Ankyloblepharon
Ankyloblepharon
18 0 3 7.3E-02 0 0