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《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)
〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
hydrogenの化学記号
鉛筆の硬度 / 《俗》heroin
乳を出す
OLD French古[代]フランス語

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1. 乳酸脱水素酵素欠損症 lactate dehydrogenase deficiency
2. 重度複合型免疫不全（SCID）：特定の欠損 severe combined immunodeficiency scid specific defects
3. 遺伝性運動失調の概要 overview of the hereditary ataxias
4. 成人における鉄欠乏性貧血の原因および診断 causes and diagnosis of iron deficiency anemia in the adult
5. ヘキソースリン酸側路およびグルタチオン代謝疾患（グルコース-6-リン酸脱水素酵素欠損症を除く） disorders of the hexose monophosphate shunt and glutathione metabolism other than glucose 6 phosphate dehydrogenase deficiency

A novel in-frame deletion mutation in a case of lactate dehydrogenase (LD) H subunit deficiency showing an atypical LD isoenzyme pattern in serum and erythrocytes.

Sudo K1, Maekawa M, Houki N, Okuda T, Akizuki S, Magara T, Kawano K.
Clinical biochemistry.Clin Biochem.1999 Mar;32(2):137-41.
OBJECTIVE: We report a case showing an atypical lactate dehydrogenase (LD) isoenzyme pattern involving deficiency only of LD-1 and LD-2 in serum and erythrocytes. LD activity in serum from this patient was extremely low, similar to complete LD-H deficiency, and also that in erythrocytes was low.DESI
PMID 10211631

Wakabayashi H1, Tsuchiya M, Yoshino K, Kaku K, Shigei H.
Internal medicine (Tokyo, Japan).Intern Med.1996 Jul;35(7):550-4.
We report herein the fifth family of hereditary deficiency of lactate dehydrogenase (LDH) H-subunit with an autosomal recessive inheritance including two cases of complete deficiency. Their LDH activities were low both in the serum and in the red blood cells (RBC). Electrophoretic analysis revealed
PMID 8842761

Kanno T1.
Rinsho byori. The Japanese journal of clinical pathology.Rinsho Byori.1991 Aug;39(8):809-13.
Detection of symptom poor hereditary disorders from laboratory data is one of the targets of the laboratory data analysis system. Symptom poor hereditary disorders include; 1) pharmacogenetic disorders, 2) heterozygous individuals of hereditary disorders, 3) early or symptomless stage of hereditary
PMID 1920875