CDAN1, codanin 1, 146059

N. diseases: 77; N. variants: 15
Disease: Secondary hemochromatosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		0.030 Biomarker disease BEFREE Congenital dyserythropoietic anemia type I (CDAI) is a rare autosomal recessive disease characterized by macrocytic anemia, ineffective erythropoiesis, and secondary hemochromatosis. 27206021 2017
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		0.030 Biomarker disease BEFREE Congenital dyserythropoietic anemia type I is an inherited autosomal recessive macrocytic anemia associated with ineffective erythropoiesis and the development of secondary hemochromatosis. 19336738 2009
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		0.030 Biomarker disease BEFREE Therapeutic measures include interferon-alpha for CDA I, splenectomy for CDA II, and iron depletion for all individuals at risk for secondary hemochromatosis. 15278299 2004