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: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome 		1 0 1 6.7E-02 0 0
CUI: C0206692
Disease: Carcinoma, Lobular
Carcinoma, Lobular 		1 0 1 6.7E-02 0 0
CUI: C0206711
Disease: Pilomatrixoma
Pilomatrixoma 		1 6 1 6.7E-02 2 5.7E-02
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia 		1 2 1 6.7E-02 1 3.1E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		1 0 1 6.7E-02 0 0
CUI: C0406709
Disease: Hay-Wells syndrome
Hay-Wells syndrome 		1 0 1 6.7E-02 0 0
CUI: C0746787
Disease: Cancer of Neck
Cancer of Neck 		1 0 1 6.7E-02 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		1 0 1 6.7E-02 0 0
CUI: C1336076
Disease: Sporadic Breast Carcinoma
Sporadic Breast Carcinoma 		1 0 1 6.7E-02 0 0
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		1 0 1 6.7E-02 0 0
CUI: C1785148
Disease: RAPP-HODGKIN SYNDROME
RAPP-HODGKIN SYNDROME 		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: C1838457
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D1
FANCONI ANEMIA, COMPLEMENTATION GROUP D1 		1 0 1 6.7E-02 0 0
CUI: C1851878
Disease: OROFACIAL CLEFT 8
OROFACIAL CLEFT 8 		1 0 1 6.7E-02 0 0
CUI: C1854442
Disease: SPLIT-HAND/FOOT MALFORMATION 4
SPLIT-HAND/FOOT MALFORMATION 4 		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: C1863204
Disease: ADULT SYNDROME
ADULT SYNDROME 		1 0 1 6.7E-02 0 0
CUI: C1865285
Disease: Megalencephaly cutis marmorata telangiectatica congenita
Megalencephaly cutis marmorata telangiectatica congenita 		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: C2751313
Disease: CLAPO Syndrome
CLAPO Syndrome 		1 3 1 6.7E-02 1 3.0E-02
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: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		1 0 1 6.7E-02 0 0
CUI: C3150971
Disease: LEOPARD SYNDROME 3
LEOPARD SYNDROME 3 		1 0 1 6.7E-02 0 0
CUI: C3554449
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 19
MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 		1 0 1 6.7E-02 0 0
CUI: C3554518
Disease: COWDEN SYNDROME 5
COWDEN SYNDROME 5 		1 0 1 6.7E-02 0 0