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: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		15 0 3 0.12 0 0
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		7 0 2 0.11 0 0
CUI: C0005426
Disease: Biliary Tract Neoplasm
Biliary Tract Neoplasm 		1 0 1 7.7E-02 0 0
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		1 0 1 7.7E-02 0 0
CUI: C0016037
Disease: Fibrodysplasia Ossificans Progressiva
Fibrodysplasia Ossificans Progressiva 		1 0 1 7.7E-02 0 0
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		1 0 1 7.7E-02 0 0
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		1 0 1 7.7E-02 0 0
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms 		1 0 1 7.7E-02 0 0
CUI: C0027533
Disease: Neck Neoplasms
Neck Neoplasms 		1 0 1 7.7E-02 0 0
CUI: C0027832
Disease: Neurofibromatosis 2
Neurofibromatosis 2 		1 0 1 7.7E-02 0 0
CUI: C0030297
Disease: Pancreatic Neoplasm
Pancreatic Neoplasm 		1 2 1 7.7E-02 1 7.7E-02
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome 		1 6 1 7.7E-02 1 5.9E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		1 0 1 7.7E-02 0 0
CUI: C0587248
Disease: Costello syndrome (disorder)
Costello syndrome (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		1 0 1 7.7E-02 0 0
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		1 0 1 7.7E-02 0 0
CUI: C1527349
Disease: Ductal Breast Carcinoma
Ductal Breast Carcinoma 		1 0 1 7.7E-02 0 0
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		1 0 1 7.7E-02 0 0
CUI: C1838457
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D1
FANCONI ANEMIA, COMPLEMENTATION GROUP D1 		1 0 1 7.7E-02 0 0
CUI: C1854416
Disease: MACROCEPHALY/AUTISM SYNDROME
MACROCEPHALY/AUTISM SYNDROME 		1 0 1 7.7E-02 0 0
CUI: C2751642
Disease: GLIOMA SUSCEPTIBILITY 2
GLIOMA SUSCEPTIBILITY 2 		1 0 1 7.7E-02 0 0
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		1 0 1 7.7E-02 0 0
CUI: C3150971
Disease: LEOPARD SYNDROME 3
LEOPARD SYNDROME 3 		1 0 1 7.7E-02 0 0
CUI: C4014738
Disease: MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 		1 3 1 7.7E-02 1 7.1E-02
CUI: C4539857
Disease: CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME 		1 0 1 7.7E-02 0 0