Disease: Achalasia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Achalasia
CUI: C1321756
Disease: Achalasia
0.010 GeneticVariation BEFREE Gender-specific association of the PTPN22 C1858T polymorphism with achalasia. 17961776 2007