Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.600 CausalMutation disease CLINVAR
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.600 CausalMutation disease CGI
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms 		0.500 CausalMutation group CGI
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms 		0.500 Biomarker group CTD_human
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.500 Biomarker disease CTD_human
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.500 CausalMutation disease CGI
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.460 Biomarker disease CTD_human
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.460 Biomarker disease HPO
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma 		0.400 Biomarker disease HPO
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.360 Biomarker disease CTD_human
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.320 Biomarker group CTD_human
CUI: C0035412
Disease: Rhabdomyosarcoma
Rhabdomyosarcoma 		0.310 GeneticVariation disease UNIPROT
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.300 GeneticVariation disease ORPHANET
CUI: C1257931
Disease: Mammary Neoplasms, Human
Mammary Neoplasms, Human 		0.300 Biomarker disease CTD_human
CUI: C1849385
Disease: Rhabdomyosarcoma 1
Rhabdomyosarcoma 1 		0.300 Biomarker disease CTD_human
CUI: C4704874
Disease: Mammary Carcinoma, Human
Mammary Carcinoma, Human 		0.300 Biomarker disease CTD_human
CUI: C0007120
Disease: Bronchioloalveolar Adenocarcinoma
Bronchioloalveolar Adenocarcinoma 		0.100 Biomarker disease HPO
CUI: C0544886
Disease: Somatic mutation
Somatic mutation 		0.100 Biomarker phenotype HPO
CUI: C4016802
Disease: RHABDOMYOSARCOMA, SOMATIC
RHABDOMYOSARCOMA, SOMATIC 		0.100 CausalMutation disease CLINVAR
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		0.010 GeneticVariation disease BEFREE - During a 2.5-year period, we compared 4 groups of patients (n = 60): FVL heterozygous (FVL-HET)/taking rivaroxaban, wild-type/taking rivaroxaban, FVL-HET/no rivaroxaban, and normal APCR/no rivaroxaban. 28920711 2018
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 Biomarker group BEFREE 15-LOX-2 was expressed in normal esophageal epithelial cells (EECs) at the highest levels, whereas an SV40-immortalized HET-1A line and three of five esophageal cancer cell lines failed to express it at detectable levels. 12659684 2003
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 Biomarker disease BEFREE 15-LOX-2 was expressed in normal esophageal epithelial cells (EECs) at the highest levels, whereas an SV40-immortalized HET-1A line and three of five esophageal cancer cell lines failed to express it at detectable levels. 12659684 2003
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 Biomarker disease BEFREE 15-LOX-2 was expressed in normal esophageal epithelial cells (EECs) at the highest levels, whereas an SV40-immortalized HET-1A line and three of five esophageal cancer cell lines failed to express it at detectable levels. 12659684 2003
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 Biomarker disease BEFREE Atherosclerosis was diagnosed by (carotid and femoral) ITM measurement and ABPI. 28146208 2017
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 Biomarker disease BEFREE Atherosclerosis was diagnosed by (carotid and femoral) ITM measurement and ABPI. 28146208 2017