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: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		579 0 4 6.4E-03 0 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		460 0 4 7.8E-03 0 0
CUI: C1335302
Disease: Pancreatic Ductal Adenocarcinoma
Pancreatic Ductal Adenocarcinoma 		11 0 1 1.6E-02 0 0
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		7 0 1 1.7E-02 0 0
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		4 0 1 1.8E-02 0 0
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		4 0 1 1.8E-02 0 0
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		3 0 1 1.8E-02 0 0
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		3 0 1 1.8E-02 0 0
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
Transitional cell carcinoma of bladder 		3 0 1 1.8E-02 0 0
CUI: C4048328
Disease: cervical cancer
cervical cancer 		3 0 1 1.8E-02 0 0
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis 		2 0 1 1.8E-02 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		2 0 1 1.8E-02 0 0
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		2 0 1 1.8E-02 0 0
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME 		2 0 1 1.8E-02 0 0
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		2 0 1 1.8E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		1 0 1 1.9E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		1 0 1 1.9E-02 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		1 0 1 1.9E-02 0 0
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		1 0 1 1.9E-02 0 0
CUI: C0024507
Disease: Majewski Syndrome
Majewski Syndrome 		1 0 1 1.9E-02 0 0
CUI: C0334634
Disease: Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse 		1 0 1 1.9E-02 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		1 0 1 1.9E-02 0 0
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		1 0 1 1.9E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		1 0 1 1.9E-02 0 0
CUI: C1852406
Disease: Cutis Gyrata Syndrome of Beare And Stevenson
Cutis Gyrata Syndrome of Beare And Stevenson 		1 0 1 1.9E-02 0 0