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01	590040	MTTH	TRANSFER RNA, MITOCHONDRIAL, HISTIDINE	-

Disease

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	MeSH term	Japanese	Link	01
	Cardiomyopathies	心筋疾患
	Hearing Loss, Sensorineural	難聴-内耳性
	Reye Syndrome	Reye症候群
	Optic Atrophy	視神経萎縮
	MERRF Syndrome	MERRF症候群
	Testicular Diseases	精巣疾患
	Optic Atrophy, Hereditary, Leber	視神経萎縮-遺伝性-Leber
	Mitochondrial Encephalomyopathies	ミトコンドリア脳筋症
	Headache	頭痛
	MELAS Syndrome	MELAS症候群
	Mitochondrial Diseases	ミトコンドリア病
	Disease Progression	病勢悪化
	Brain Edema	脳浮腫
	Ataxia	運動失調症
	Hypogonadism	性機能低下症
	Muscular Diseases	筋疾患
	Cataract	白内障
	Seizures	けいれん性発作
	Retinitis Pigmentosa	網膜色素変性症
	Genetic Predisposition to Disease	遺伝的素因(疾患)

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Chemicals

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	MeSH term	Japanese	Link	01
	RNA, Transfer, His	ヒスチジンtRNA
	DNA, Mitochondrial	ミトコンドリアDNA
	NADH Dehydrogenase	シトクロムcレダクターゼ
	Cyclooxygenase 1	COX-1遺伝子産物
	Succinate Dehydrogenase	コハク酸オキシダーゼ
	Electron Transport Complex IV	電子伝達複合体IV
	Prostaglandin-Endoperoxide Synthases	Prostaglandin-Endoperoxide Synthases
	Cyclooxygenase 2	COX-2遺伝子産物
	Isoenzymes	アイソエンザイム
	Membrane Proteins	膜蛋白質

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Biological Phenomena

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	MeSH term	Japanese	Link	01
	Nucleic Acid Conformation	核酸高次構造
	Mutation	変異
	Phenotype	表現型
	Genetic Variation	遺伝的多様性
	Evolution, Molecular	分子進化
	Genetic Testing	遺伝学的スクリーニング
	Polymorphism, Single-Stranded Conformational	PCR-SSCP法
	Phylogeny	系統発生
	Conserved Sequence	保存配列
	Amino Acid Substitution	アミノ酸置換
	Sequence Homology, Nucleic Acid	核酸配列相同性
	Genetic Predisposition to Disease	遺伝的素因(疾患)
	Point Mutation	点変異
	Immunohistochemistry	免疫組織化学
	Base Sequence	塩基配列

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Anatomy

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	MeSH term	Japanese	Link	01
	Muscle Fibers, Fast-Twitch	F型筋線維
	Mitochondria	ミトコンドリア
	Muscle, Skeletal	骨格筋
	Muscle Fibers, Skeletal	筋線維
	Cytoplasm	細胞質
	Brain	脳

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Organisms

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	MeSH term	Japanese	Link	01
	Humans	ヒト

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Database Center for Life Science