PRCP, prolylcarboxypeptidase, 5547

N. diseases: 68; N. variants: 7
Disease: Spina Bifida ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		0.020 GeneticVariation disease BEFREE Homozygous disruption of PCP genes in mice results in a spectrum of NTDs, including defects that affect the entire neural axis (craniorachischisis), cranial NTDs (exencephaly) and spina bifida. 21840926 2011
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		0.020 GeneticVariation disease BEFREE We used data from a case-control study conducted in California to evaluate the association between variation within several key PCP genes and the risk of spina bifida. 20101694 2010