Disease: Hamartoma Syndrome, Multiple ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		0.010 PosttranslationalModification disease BEFREE DNA methylation of TCERG1L in 101 serum samples of CD patients was examined. 24317008 2014