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: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		2 0 1 1.8E-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: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung 		32 0 5 6.2E-02 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		1 0 1 1.9E-02 0 0
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		3 0 1 1.8E-02 0 0
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		10 0 1 1.6E-02 0 0
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		4 0 1 1.8E-02 0 0
CUI: C0796237
Disease: Mental Retardation, X-Linked 30
Mental Retardation, X-Linked 30 		1 0 1 1.9E-02 0 0
CUI: C1136033
Disease: Cutaneous Mastocytosis
Cutaneous Mastocytosis 		1 0 1 1.9E-02 0 0
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		15 0 1 1.5E-02 0 0
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		7 0 3 5.2E-02 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		1 19 1 1.9E-02 1 1.7E-02
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		4 0 1 1.8E-02 0 0
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		1 0 1 1.9E-02 0 0
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma 		31 0 5 6.2E-02 0 0
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		23 0 4 5.5E-02 0 0
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		4 0 2 3.6E-02 0 0
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		31 0 2 2.4E-02 0 0
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		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: C1849334
Disease: Robinow syndrome, autosomal recessive
Robinow syndrome, autosomal recessive 		1 0 1 1.9E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		1 0 1 1.9E-02 0 0
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		1 0 1 1.9E-02 0 0
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		1 0 1 1.9E-02 0 0
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome 		1 0 1 1.9E-02 0 0