CDA, cytidine deaminase, 978

N. diseases: 103; N. variants: 9
Disease: hereditary anemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0850672
Disease: hereditary anemia
hereditary anemia 		0.010 Biomarker disease BEFREE CDA type I is a rare hereditary anemia, characterized by relative reticulocytopenia, and congenital anomalies. 31191338 2019