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・ Congenital clasped thumb
・ Congenital contractural arachnodactyly
・ Congenital contractural arachnodactyly in cattle
・ Congenital cutaneous candidiasis
・ Congenital cytomegalovirus infection
・ Congenital dermal sinus
・ Congenital diaphragmatic hernia
・ Congenital disorder
・ Congenital disorder of glycosylation
・ Congenital disorder of glycosylation type IIc
・ Congenital disorders of amino acid metabolism
・ Congenital distal spinal muscular atrophy
・ Congenital dyserythropoietic anemia
・ Congenital dyserythropoietic anemia type I
・ Congenital dyserythropoietic anemia type II
Congenital dyserythropoietic anemia type III
・ Congenital dyserythropoietic anemia type IV
・ Congenital epulis
・ Congenital erosive and vesicular dermatosis
・ Congenital estrogen deficiency
・ Congenital fiber type disproportion
・ Congenital fibrosis of the extraocular muscles
・ Congenital fourth nerve palsy
・ Congenital generalized lipodystrophy
・ Congenital hearing loss
・ Congenital heart defect
・ Congenital Heart Surgeons' Society
・ Congenital hemolytic anemia
・ Congenital hepatic fibrosis
・ Congenital hereditary endothelial dystrophy


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Congenital dyserythropoietic anemia 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.

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