Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0859976
Disease: Idiopathic achalasia of esophagus
Idiopathic achalasia of esophagus
0.300 GermlineCausalMutation disease ORPHANET Truncating mutation in the nitric oxide synthase 1 gene is associated with infantile achalasia. 25479138 2015