PER2, period circadian regulator 2, 8864

N. diseases: 238; N. variants: 15
Disease: Methylcrotonyl-CoA carboxylase deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551505
Disease: Methylcrotonyl-CoA carboxylase deficiency
Methylcrotonyl-CoA carboxylase deficiency 		0.010 GeneticVariation disease BEFREE During the study period, 2,959,108 infants were screened and 71 infants were diagnosed with 3-MCCD for an overall incidence of 1:41,676. 24103308 2013