Source: UNIPROT ×
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: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		54 0 1 1.5E-02 0 0
CUI: C1863204
Disease: ADULT SYNDROME
ADULT SYNDROME 		1 0 1 6.7E-02 0 0
CUI: C4012790
Disease: Ataxia-Telangiectasisa-Like Disorder 1
Ataxia-Telangiectasisa-Like Disorder 1 		1 0 1 6.7E-02 0 0
CUI: C4551988
Disease: BLEPHAROCHEILODONTIC SYNDROME 1
BLEPHAROCHEILODONTIC SYNDROME 1 		1 0 1 6.7E-02 0 0
CUI: C2676676
Disease: BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		1 5 1 6.7E-02 1 2.9E-02
CUI: C0746787
Disease: Cancer of Neck
Cancer of Neck 		1 0 1 6.7E-02 0 0
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		10 0 3 0.14 0 0
CUI: C0206692
Disease: Carcinoma, Lobular
Carcinoma, Lobular 		1 0 1 6.7E-02 0 0
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		2 2 2 0.13 2 6.5E-02
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		1 0 1 6.7E-02 0 0
CUI: C4048328
Disease: cervical cancer
cervical cancer 		3 0 2 0.12 0 0
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		1 0 1 6.7E-02 0 0
CUI: C2751313
Disease: CLAPO Syndrome
CLAPO Syndrome 		1 3 1 6.7E-02 1 3.0E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		460 370 4 8.5E-03 1 2.5E-03
CUI: C2752042
Disease: Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 		1 2 1 6.7E-02 1 3.1E-02
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia 		1 2 1 6.7E-02 1 3.1E-02
CUI: C3554518
Disease: COWDEN SYNDROME 5
COWDEN SYNDROME 5 		1 0 1 6.7E-02 0 0
CUI: C4310801
Disease: DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR
DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR 		1 0 1 6.7E-02 0 0
CUI: C1858562
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3 		1 0 1 6.7E-02 0 0
CUI: C4539767
Disease: EXUDATIVE VITREORETINOPATHY 7
EXUDATIVE VITREORETINOPATHY 7 		1 0 1 6.7E-02 0 0
CUI: C1838457
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D1
FANCONI ANEMIA, COMPLEMENTATION GROUP D1 		1 0 1 6.7E-02 0 0
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		1 0 1 6.7E-02 0 0
CUI: C4554406
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP S
FANCONI ANEMIA, COMPLEMENTATION GROUP S 		1 2 1 6.7E-02 1 3.1E-02
CUI: C2750850
Disease: GLIOMA SUSCEPTIBILITY 1
GLIOMA SUSCEPTIBILITY 1 		5 0 1 5.3E-02 0 0
CUI: C0406709
Disease: Hay-Wells syndrome
Hay-Wells syndrome 		1 0 1 6.7E-02 0 0