WordNet

(baseball) a failure of a defensive player to make an out when normal play would have sufficed (同)misplay
departure from what is ethically acceptable (同)wrongdoing
(computer science) the occurrence of an incorrect result produced by a computer (同)computer error
a misconception resulting from incorrect information (同)erroneous belief
part of a statement that is not correct; "the book was full of errors" (同)mistake
to make a mistake or be incorrect (同)mistake, slip
a simple sugar found in honey and in many ripe fruits (同)fruit_sugar, levulose, laevulose
the organic processes (in a cell or organism) that are necessary for life (同)metabolic_process

PrepTutorEJDIC

《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
〈C〉『誤り』,『まちがい』 / 〈U〉思い違い,誤解 / 〈U〉〈C〉過ち,過失 / 〈U〉(計数の)誤差 / 〈C〉(野球で)エラー,失策
(判断・考え方・選択などで)『誤る』,まちがえる;過ちを犯す,罪を犯す《+『in』+『名』(do『ing』)》 / (正道・目的などから)それる,逸脱する《+『from』+『名』》
〈U〉果糖
新陳代謝,物質交代

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 先天性代謝異常：分類 inborn errors of metabolism classification
2. 先天性代謝異常：個々の障害の発見 inborn errors of metabolism identifying the specific disorder
3. 先天性代謝異常：代謝性救急疾患 inborn errors of metabolism metabolic emergencies
4. 先天性代謝異常：疫学、病因、および臨床的特徴 inborn errors of metabolism epidemiology pathogenesis and clinical features
5. 新生児低血糖の病因、スクリーニング、および診断 pathogenesis screening and diagnosis of neonatal hypoglycemia

Kamate M1, Jambagi M1, Gowda P1, Sonoli S1.
BMJ case reports.BMJ Case Rep.2014 Sep 22;2014. pii: bcr2013201553. doi: 10.1136/bcr-2013-201553.
Fructose-1,6-diphosphatase (FDPase) deficiency is usually considered an inborn error of fructose metabolism, however, strictly speaking it is a defect of gluconeogenesis. The disorder is manifested by the appearance of hypoglycaemia, ketosis and lactic acidosis (neonatally or later during fasting or
PMID 25246452

D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK).

Sass JO1, Fischer K, Wang R, Christensen E, Scholl-Bürgi S, Chang R, Kapelari K, Walter M.
Human mutation.Hum Mutat.2010 Dec;31(12):1280-5. doi: 10.1002/humu.21375. Epub 2010 Nov 9.
D-glyceric aciduria is a rare inborn error of serine and fructose metabolism that was first described in 1974. Most affected individuals have presented with neurological symptoms. The molecular basis of D-glyceric aciduria is largely unknown; possible causes that have been discussed are deficiencies
PMID 20949620

Fructose 1,6-bisphosphatase deficiency: enzyme and mutation analysis performed on calcitriol-stimulated monocytes with a note on long-term prognosis.

Åsberg C1, Hjalmarson O, Alm J, Martinsson T, Waldenström J, Hellerud C.
Journal of inherited metabolic disease.J Inherit Metab Dis.2010 Dec;33 Suppl 3:S113-21. doi: 10.1007/s10545-009-9034-5. Epub 2010 Feb 12.
Fructose 1,6-bisphosphatase (FBPase) deficiency is an inborn error of metabolism in the gluconeogenetic pathway. During periods of low food intake or infections, a defect in FBPase can result in hypoglycemia, ketonuria and metabolic acidosis. We established a diagnostic system for FBPase deficiency
PMID 20151204