Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0201952
Disease: Chloride measurement
Chloride measurement 		0.100 GeneticVariation phenotype GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
CUI: C0202194
Disease: Potassium measurement
Potassium measurement 		0.100 GeneticVariation phenotype GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
CUI: C3893645
Disease: response to ACE inhibitor
response to ACE inhibitor 		0.100 GeneticVariation phenotype GWASCAT Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population. 28084903 2017
CUI: C0004096
Disease: Asthma
Asthma 		0.100 CausalMutation disease CLINVAR
CUI: C0004096
Disease: Asthma
Asthma 		0.100 GeneticVariation disease CLINVAR
CUI: C0017152
Disease: Gastritis
Gastritis 		0.100 CausalMutation disease CLINVAR
CUI: C0017152
Disease: Gastritis
Gastritis 		0.100 GeneticVariation disease CLINVAR
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation phenotype CLINVAR
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0152020
Disease: Gastroparesis
Gastroparesis 		0.100 GeneticVariation disease CLINVAR
CUI: C0152020
Disease: Gastroparesis
Gastroparesis 		0.100 CausalMutation disease CLINVAR
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		0.100 CausalMutation phenotype CLINVAR
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		0.100 CausalMutation phenotype CLINVAR
CUI: C0239234
Disease: Low set ears
Low set ears 		0.100 CausalMutation disease CLINVAR
CUI: C0239234
Disease: Low set ears
Low set ears 		0.100 GeneticVariation disease CLINVAR
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		0.100 CausalMutation disease CLINVAR
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		0.100 GeneticVariation disease CLINVAR
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		0.100 GeneticVariation disease CLINVAR
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		0.100 CausalMutation disease CLINVAR
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.100 GeneticVariation disease CLINVAR
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.100 CausalMutation disease CLINVAR
CUI: C0740852
Disease: Upper airway obstruction
Upper airway obstruction 		0.100 CausalMutation disease CLINVAR
CUI: C0740852
Disease: Upper airway obstruction
Upper airway obstruction 		0.100 GeneticVariation disease CLINVAR