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01 608779 CDG2E CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe - OMIM


Disease : Chemicals : Biological Phenomena : Anatomy : Organisms

Disease

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MeSH term Japanese Link 01
Carbohydrate Metabolism, Inborn Errors 炭水化物代謝異常-先天性 MeSH lifesciencedb.jp



Chemicals

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MeSH term Japanese Link 01
DNA, Complementary 相補的DNA MeSH lifesciencedb.jp
Carrier Proteins 担体蛋白質 MeSH lifesciencedb.jp



Biological Phenomena

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MeSH term Japanese Link 01
Glycosylation - MeSH lifesciencedb.jp
Homozygote ホモ接合体 MeSH lifesciencedb.jp
Base Sequence 塩基配列 MeSH lifesciencedb.jp
Mutation 変異 MeSH lifesciencedb.jp



Anatomy

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MeSH term Japanese Link 01
Golgi Apparatus Golgi装置 MeSH lifesciencedb.jp



Organisms

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MeSH term Japanese Link 01
Humans ヒト MeSH lifesciencedb.jp



Database Center for Life Science