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| CDA Type III ： ウィキペディア英語版 |
Congenital dyserythropoietic anemia type III
Congenital dyserythropoietic anemia type III (CDA III) is a rare autosomal dominant disorder characterized by macrocytic anemia, bone marrow erythroid hyperplasia and giant multlnucleate erythroblasts.〔http://hmg.oxfordjournals.org/content/4/1/109.abstract〕 New evidence suggests that this may be passed on recessively as well.
==Genetics==
CDA type III is transmitted autosomal dominantly. The genetic cause of CDA type III is known to be a problem with the KIF23 gene, located on the long arm of chromosome 15 at a position designated 15q22.
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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