Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0345893
Disease: Juvenile polyposis syndrome
Juvenile polyposis syndrome 		1.000 Biomarker disease CTD_human
CUI: C0345893
Disease: Juvenile polyposis syndrome
Juvenile polyposis syndrome 		1.000 Biomarker disease MGD
CUI: C1832940
Disease: JUVENILE POLYPOSIS OF STOMACH
JUVENILE POLYPOSIS OF STOMACH 		0.800 Biomarker disease MGD
CUI: C1832940
Disease: JUVENILE POLYPOSIS OF STOMACH
JUVENILE POLYPOSIS OF STOMACH 		0.800 Biomarker disease CTD_human
CUI: C1868081
Disease: Juvenile Polyposis Coli
Juvenile Polyposis Coli 		0.800 Biomarker disease MGD
CUI: C1868081
Disease: Juvenile Polyposis Coli
Juvenile Polyposis Coli 		0.800 Biomarker disease CTD_human
CUI: C1864730
Disease: Polyposis Syndrome, Hereditary Mixed, 2
Polyposis Syndrome, Hereditary Mixed, 2 		0.500 Biomarker disease CTD_human
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.340 Biomarker disease GENOMICS_ENGLAND
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.300 GeneticVariation disease UNIPROT
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.300 GeneticVariation disease UNIPROT
CUI: C3714239
Disease: Bmpr1a-Related Juvenile Polyposis
Bmpr1a-Related Juvenile Polyposis 		0.300 Biomarker disease CTD_human
CUI: C3714240
Disease: Smad4-Related Juvenile Polyposis
Smad4-Related Juvenile Polyposis 		0.300 Biomarker disease CTD_human
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		0.200 Biomarker disease MGD
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		0.200 Biomarker disease MGD
CUI: C0157946
Disease: Osteoarthrosis, localized, not specified whether primary or secondary
Osteoarthrosis, localized, not specified whether primary or secondary 		0.200 Biomarker disease MGD
CUI: C0392470
Disease: Anomalous atrioventricular excitation
Anomalous atrioventricular excitation 		0.200 Biomarker phenotype MGD
CUI: C2677102
Disease: Chromosome 10q23 Deletion Syndrome
Chromosome 10q23 Deletion Syndrome 		0.200 Biomarker phenotype MGD
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.130 CausalMutation disease CLINVAR
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.120 Biomarker disease HPO
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.120 CausalMutation disease CLINVAR
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.120 Biomarker disease HPO
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms 		0.110 Biomarker group HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.110 Biomarker disease HPO
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.110 Biomarker group HPO
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.110 Biomarker disease HPO