Disease: Choline Deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008412
Disease: Choline Deficiency
Choline Deficiency 		0.010 GeneticVariation disease LHGDN Genetic variation of folate-mediated one-carbon transfer pathway predicts susceptibility to choline deficiency in humans. 16236726 2005