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・ Methylisopropyllysergamide
・ Methylisopropyltryptamine
・ Methylisothiazolinone
・ Methylisothiazolone
・ Methylitaconate Delta-isomerase
・ Methylketobemidone
・ Methylliberine
・ Methyllinderone
・ Methyllithium
・ Methyllycaconitine
・ Methyllysine
・ Methylmagnesium chloride
・ Methylmalonate semialdehyde dehydrogenase
・ Methylmalonate-semialdehyde dehydrogenase (acylating)
・ Methylmalonic acid
Methylmalonic acidemia
・ Methylmalonyl CoA epimerase
・ Methylmalonyl-CoA
・ Methylmalonyl-CoA carboxytransferase
・ Methylmalonyl-CoA decarboxylase
・ Methylmalonyl-CoA mutase
・ Methylmalonyl-CoA mutase deficiency
・ Methylmercuric dicyanamide
・ Methylmercury
・ Methylmescaline
・ Methylmethaqualone
・ Methylmethcathinone
・ Methylnaltrexone
・ Methylnaphthalene
・ Methylnitronitrosoguanidine


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Methylmalonic acidemia : ウィキペディア英語版
Methylmalonic acidemia

Methylmalonic acidemia (MMA), also called methylmalonic aciduria, is an autosomal recessive metabolic disorder.〔http://www.genome.gov/19016901〕 It is a classical type of organic acidemia.
Methylmalonic acidemia stems from several genotypes, all forms of the disorder usually diagnosed in the early neonatal period, presenting progressive encephalopathy, and secondary hyperammonemia. The disorder can result in death if undiagnosed or left untreated.
==Causes==


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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