Source: INFERRED ×
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) 		8 17 4 0.11 5 3.4E-02
CUI: C1849677
Disease: Numerous nevi
Numerous nevi 		8 0 4 0.11 0 0
CUI: C0027651
Disease: Neoplasms
Neoplasms 		70 98 10 0.11 9 4.0E-02
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		19 36 5 0.11 10 6.2E-02
CUI: C3501843
Disease: Nonmedullary Thyroid Carcinoma
Nonmedullary Thyroid Carcinoma 		9 0 4 0.11 0 0
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		62 25 9 0.10 1 6.3E-03
CUI: C0206686
Disease: Adrenocortical carcinoma
Adrenocortical carcinoma 		20 34 5 0.10 19 0.13
CUI: C0265319
Disease: Fibrous skin tumor of tuberous sclerosis
Fibrous skin tumor of tuberous sclerosis 		20 0 5 0.10 0 0
CUI: C0023798
Disease: Lipoma
Lipoma 		23 0 5 9.8E-02 0 0
CUI: C0206682
Disease: Follicular thyroid carcinoma
Follicular thyroid carcinoma 		14 0 4 9.3E-02 0 0
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		26 102 5 9.3E-02 53 0.29
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		38 128 6 9.2E-02 10 4.0E-02
CUI: C0014474
Disease: Ependymoma
Ependymoma 		15 0 4 9.1E-02 0 0
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease 		3 58 3 9.1E-02 3 1.6E-02
CUI: C1834711
Disease: CEREBELLOPARENCHYMAL DISORDER VI
CEREBELLOPARENCHYMAL DISORDER VI 		3 56 3 9.1E-02 3 1.6E-02
CUI: C1834712
Disease: Cerebellar Granule Cell Hypertrophy and Megalencephaly
Cerebellar Granule Cell Hypertrophy and Megalencephaly 		3 56 3 9.1E-02 3 1.6E-02
CUI: C1866376
Disease: Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor 		3 56 3 9.1E-02 3 1.6E-02
CUI: C1866398
Disease: Proteus-Like Syndrome (disorder)
Proteus-Like Syndrome (disorder) 		3 56 3 9.1E-02 3 1.6E-02
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
PTEN Hamartoma Tumor Syndrome 		3 193 3 9.1E-02 3 9.2E-03
CUI: C2732838
Disease: Neoplasm of skeletal system
Neoplasm of skeletal system 		15 0 4 9.1E-02 0 0
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		15 33 4 9.1E-02 7 4.3E-02
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		4 98 3 8.8E-02 6 2.6E-02
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		67 6385 8 8.7E-02 34 5.2E-03
CUI: C4021977
Disease: Visceral angiomatosis
Visceral angiomatosis 		17 0 4 8.7E-02 0 0
CUI: C0018920
Disease: Hemangioma, Cavernous
Hemangioma, Cavernous 		31 0 5 8.5E-02 0 0