Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551774
Disease: FEINGOLD SYNDROME 1
FEINGOLD SYNDROME 1 		0.710 GeneticVariation disease CLINVAR
CUI: C4551774
Disease: FEINGOLD SYNDROME 1
FEINGOLD SYNDROME 1 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.700 Biomarker disease ORPHANET
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.700 GenomicAlterations disease CGI
CUI: C0796068
Disease: Oculodigitoesophagoduodenal syndrome
Oculodigitoesophagoduodenal syndrome 		0.650 CausalMutation disease CLINVAR
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C2931189
Disease: Neural crest tumor
Neural crest tumor 		0.300 Biomarker disease ORPHANET
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.130 Biomarker disease HPO
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia 		0.110 Biomarker disease HPO
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia 		0.110 GeneticVariation disease CLINVAR
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.110 Biomarker group HPO
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		0.100 Biomarker disease HPO
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		0.100 Biomarker disease HPO
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis 		0.100 CausalMutation disease CLINVAR
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		0.100 Biomarker phenotype HPO
CUI: C0025990
Disease: Micrognathism
Micrognathism 		0.100 CausalMutation disease CLINVAR
CUI: C0025990
Disease: Micrognathism
Micrognathism 		0.100 Biomarker disease HPO
CUI: C0027766
Disease: Nervous System Neoplasms
Nervous System Neoplasms 		0.100 Biomarker group HPO
CUI: C0039075
Disease: Syndactyly
Syndactyly 		0.100 CausalMutation disease CLINVAR
CUI: C0040588
Disease: Tracheoesophageal Fistula
Tracheoesophageal Fistula 		0.100 Biomarker disease HPO
CUI: C0042928
Disease: Vocal Cord Paralysis
Vocal Cord Paralysis 		0.100 Biomarker disease HPO
CUI: C0149955
Disease: Annular pancreas
Annular pancreas 		0.100 Biomarker disease HPO
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		0.100 Biomarker phenotype HPO
CUI: C0239234
Disease: Low set ears
Low set ears 		0.100 Biomarker disease HPO
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		0.100 Biomarker disease HPO