Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
1.000 CausalMutation disease CGI
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
1.000 Biomarker disease CTD_human
CUI: C1306837
Disease: Papillary Renal Cell Carcinoma
Papillary Renal Cell Carcinoma
0.800 CausalMutation disease CGI
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GeneticVariation disease UNIPROT
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 GenomicAlterations disease CGI
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.600 GenomicAlterations disease CGI
Conventional (Clear Cell) Renal Cell Carcinoma
0.600 CausalMutation disease CGI
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.580 GenomicAlterations group CGI
CUI: C4084709
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 97
DEAFNESS, AUTOSOMAL RECESSIVE 97
0.510 Biomarker disease CTD_human
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.400 CausalMutation group CGI
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.400 GenomicAlterations disease CGI
Hereditary Papillary Renal Carcinoma
0.400 GermlineCausalMutation disease ORPHANET
Squamous cell carcinoma of the head and neck
0.400 CausalMutation disease CGI
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney
0.390 Biomarker disease GENOMICS_ENGLAND
CUI: C0154060
Disease: Carcinoma in situ of stomach
Carcinoma in situ of stomach
0.310 GenomicAlterations disease CGI
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.310 GenomicAlterations disease CGI
CUI: C1709353
Disease: Osteofibrous Dysplasia
Osteofibrous Dysplasia
0.310 Biomarker disease CTD_human
CUI: C0153943
Disease: Benign neoplasm of stomach
Benign neoplasm of stomach
0.300 GenomicAlterations disease CGI
Neoplasm of uncertain or unknown behavior of stomach
0.300 GenomicAlterations disease CGI
Papillary renal cell carcinoma, familial
0.300 GermlineCausalMutation disease ORPHANET
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum
0.300 GermlineCausalMutation disease ORPHANET Familial congenital bowing of the tibia with pseudarthrosis and pectus excavatum: report of a kindred. 1270474 1976
OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO
0.300 GermlineCausalMutation phenotype ORPHANET Familial congenital bowing of the tibia with pseudarthrosis and pectus excavatum: report of a kindred. 1270474 1976
CUI: C1306837
Disease: Papillary Renal Cell Carcinoma
Papillary Renal Cell Carcinoma
0.800 Biomarker disease CLINGEN The receptor encoded by the human c-MET oncogene is expressed in hepatocytes, epithelial cells and solid tumors. 1917129 1991
Papillary renal cell carcinoma, sporadic
0.300 Biomarker disease CLINGEN The receptor encoded by the human c-MET oncogene is expressed in hepatocytes, epithelial cells and solid tumors. 1917129 1991
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum
0.300 GermlineCausalMutation disease ORPHANET Osteofibrous dysplasia: clinicopathologic study of 80 cases. 8276381 1993