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01 607200 - THYROID HORMONOGENESIS, GENETIC DEFECT IN, 6 - OMIM


Disease : Chemicals : Biological Phenomena : Anatomy : Organisms

Disease

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 MeSH term Japanese Link 01
Congenital Hypothyroidism クレチン症 MeSH lifesciencedb.jp
Hypothyroidism 甲状腺機能低下症 MeSH lifesciencedb.jp
Thyroid Dysgenesis 甲状腺発育不全 MeSH lifesciencedb.jp


Chemicals

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 MeSH term Japanese Link 01
Flavoproteins フラビン蛋白質 MeSH lifesciencedb.jp
NADPH Oxidase NADPHオキシダーゼ MeSH lifesciencedb.jp
Thyroid Hormones 甲状腺ホルモン MeSH lifesciencedb.jp
Receptors, Thyrotropin 甲状腺刺激ホルモン受容体 MeSH lifesciencedb.jp
Hydrogen Peroxide 過酸化水素 MeSH lifesciencedb.jp
Forkhead Transcription Factors FKH遺伝子産物 MeSH lifesciencedb.jp
Repressor Proteins レプレッサー蛋白質 MeSH lifesciencedb.jp


Biological Phenomena

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 MeSH term Japanese Link 01
Amino Acid Sequence アミノ酸配列 MeSH lifesciencedb.jp
Neonatal Screening 新生児スクリーニング MeSH lifesciencedb.jp
Mutation 変異 MeSH lifesciencedb.jp
Genetic Variation 遺伝的多様性 MeSH lifesciencedb.jp
Phenotype 表現型 MeSH lifesciencedb.jp


Anatomy

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 MeSH term Japanese Link 01


Organisms

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 MeSH term Japanese Link 01
Animals 動物 MeSH lifesciencedb.jp
Humans ヒト MeSH lifesciencedb.jp


Database Center for Life Science