CDA, cytidine deaminase, 978

N. diseases: 103; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.040 GeneticVariation phenotype BEFREE Furthermore, the association of two linked cytidine deaminase (CDA) promoter variants (c.1-451C>T: OR<sub>dominant</sub> = 4.3, 95% CI 1.3-14.2, P<sub>adjusted</sub> = 0.017; and c.1-92A>G: OR<sub>dominant</sub> = 4.4, 95% CI 1.3-14.5, P<sub>adjusted</sub> = 0.015) with Cp-related diarrhea was replicated. 28139840 2017
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.040 GeneticVariation phenotype BEFREE The linked CDA c.-92A>G and CDA c.-451C>T variants predicted grade 2-4 diarrhoea (P=0.0055, OR=2.3, 95% CI: 1.3-4.2 and P=0.0082, OR=2.3, 95% CI: 1.3-4.2, respectively). 23736036 2013
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.040 GeneticVariation phenotype BEFREE The presence of two polymorphisms (CDD 943insC and CES 2 Exon3 6046 G/A) were associated with a non-statistically significant higher incidence of grade 3 hand-foot syndrome (HFS) (p=0.07) and grade 3-4 diarrhoea (p=0.09), respectively. 18473752 2008
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.040 GeneticVariation phenotype BEFREE Southern blot analysis was performed with a probe specific for the cda gene of pColD157 and two groups of EHEC O157:H7 isolates from patients with diarrhea or hemolytic-uremic syndrome resident in Germany. 9431914 1998