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01 300475 - CONTIGUOUS ABCD1/DXS1375E DELETION SYNDROME - OMIM


Disease : Chemicals : Biological Phenomena : Anatomy : Organisms

Disease

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 MeSH term Japanese Link 01
Peroxisomal Disorders ペルオキシソーム病 MeSH lifesciencedb.jp
Infant, Newborn, Diseases 新生児疾患 MeSH lifesciencedb.jp
Adrenoleukodystrophy 副腎白質ジストロフィー MeSH lifesciencedb.jp
Syndrome 症候群 MeSH lifesciencedb.jp


Chemicals

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 MeSH term Japanese Link 01
Chemokine CCL22 - MeSH lifesciencedb.jp
Chemokines, CC ケモカインCC MeSH lifesciencedb.jp
ATP-Binding Cassette Transporters ABCトランスポーター MeSH lifesciencedb.jp
Proteins 蛋白質 MeSH lifesciencedb.jp
Membrane Proteins 膜蛋白質 MeSH lifesciencedb.jp


Biological Phenomena

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 MeSH term Japanese Link 01
Promoter Regions, Genetic プロモーター領域 MeSH lifesciencedb.jp
Sequence Deletion 配列欠失 MeSH lifesciencedb.jp
Age of Onset 発病年齢 MeSH lifesciencedb.jp
X Chromosome X染色体 MeSH lifesciencedb.jp
Exons エクソン MeSH lifesciencedb.jp
Heterozygote ヘテロ接合体 MeSH lifesciencedb.jp
Phenotype 表現型 MeSH lifesciencedb.jp


Anatomy

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 MeSH term Japanese Link 01
Peroxisomes ペルオキシソーム MeSH lifesciencedb.jp
X Chromosome X染色体 MeSH lifesciencedb.jp
Fibroblasts 線維芽細胞 MeSH lifesciencedb.jp


Organisms

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 MeSH term Japanese Link 01
Humans ヒト MeSH lifesciencedb.jp


Database Center for Life Science