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・ Histhan Mandali
・ Histia
・ Histia flabellicornis
・ Histiaea
・ Histiaeotis
・ Histiaeus
・ Histidine
・ Histidine (data page)
・ Histidine ammonia-lyase
・ Histidine decarboxylase
・ Histidine kinase
・ Histidine N-acetyltransferase
・ Histidine operon leader
・ Histidine transaminase
・ Histidine-tryptophan-ketoglutarate
Histidinemia
・ Histidine—tRNA ligase
・ Histidinol dehydrogenase
・ Histidinol-phosphatase
・ Histidinol-phosphate transaminase
・ Histiobranchus
・ Histiocyte
・ Histiocytic sarcoma
・ Histiocytoma
・ Histiocytoma (dog)
・ Histiocytosis
・ Histiodraco velifer
・ Histioea
・ Histioea amazonica
・ Histioea bellatrix


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Histidinemia : ウィキペディア英語版
Histidinemia

Histidinemia, also referred to as histidinuria, is a rare autosomal recessive metabolic disorder caused by a deficiency of the enzyme histidase. Histidase is needed for the metabolism of the amino acid histidine. Although originally thought to be linked to multiple developmental disorders histidinemia is now accepted as a relatively benign disorder,〔 leading to a reduction in the prevalence of neonatal screening procedures.〔
==Prevalence==

Histidinemia is a rare autosomal recessive disorder. However, histidinemia is considered the most prevalent inborn error of metabolism with a reported incidence of 1:8600 (Quebec); 1:180,000 (New York) and 1:9600 (Japan); and an average of 1:12,000 observed in the neonatal screening of over 20 million newborns.〔

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