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01 610768 CDG1M CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im - OMIM


Disease : Chemicals : Biological Phenomena : Anatomy : Organisms

Disease

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MeSH term Japanese Link 01
Cardiomyopathy, Dilated 心筋症-拡張型 MeSH lifesciencedb.jp
Genetic Diseases, Inborn 遺伝性疾患 MeSH lifesciencedb.jp



Chemicals

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MeSH term Japanese Link 01
Dolichol Phosphates ドリコールリン酸 MeSH lifesciencedb.jp
Phosphotransferases (Alcohol Group Acceptor) ホスホトランスフェラーゼ(アルコール基アクセプター) MeSH lifesciencedb.jp



Biological Phenomena

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MeSH term Japanese Link 01
Glycosylation - MeSH lifesciencedb.jp
Phenotype 表現型 MeSH lifesciencedb.jp
Mutation 変異 MeSH lifesciencedb.jp



Anatomy

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MeSH term Japanese Link 01
Skin 皮膚 MeSH lifesciencedb.jp
Fibroblasts 線維芽細胞 MeSH lifesciencedb.jp
Cells, Cultured 培養細胞 MeSH lifesciencedb.jp



Organisms

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MeSH term Japanese Link 01
Saccharomyces cerevisiae 酵母-パン MeSH lifesciencedb.jp
Humans ヒト MeSH lifesciencedb.jp



Database Center for Life Science