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01 161000 - NAEGELI SYNDROME - OMIM


Disease : Chemicals : Biological Phenomena : Anatomy : Organisms

Disease

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MeSH term Japanese Link 01
Ectodermal Dysplasia 外胚葉異形成症 MeSH lifesciencedb.jp
Hyperpigmentation 色素沈着過度 MeSH lifesciencedb.jp
Hypohidrosis 発汗減少 MeSH lifesciencedb.jp
Pigmentation Disorders 色素異常症 MeSH lifesciencedb.jp
Acantholysis 棘融解 MeSH lifesciencedb.jp
Skin Diseases, Genetic 皮膚疾患-遺伝性 MeSH lifesciencedb.jp
Nevus, Pigmented 母斑-色素性 MeSH lifesciencedb.jp
Keratoderma, Palmoplantar 掌蹠角皮症 MeSH lifesciencedb.jp
Syndrome 症候群 MeSH lifesciencedb.jp



Chemicals

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MeSH term Japanese Link 01
Keratins ケラチン MeSH lifesciencedb.jp
Keratins, Type I Keratins, Type I MeSH lifesciencedb.jp
Keratin-14 ケラチン-14 MeSH lifesciencedb.jp
gamma Catenin ガンマ-カテニン MeSH lifesciencedb.jp
Keratin-5 ケラチン-5 MeSH lifesciencedb.jp
Desmoplakins デスモプラキン MeSH lifesciencedb.jp
Codon, Nonsense ナンセンスコドン MeSH lifesciencedb.jp
Cytoskeletal Proteins 細胞骨格蛋白質 MeSH lifesciencedb.jp
DNA, Complementary 相補的DNA MeSH lifesciencedb.jp



Biological Phenomena

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MeSH term Japanese Link 01
Genes, Dominant 優性遺伝子 MeSH lifesciencedb.jp
Chromosomes, Human, Pair 17 ヒト第17染色体 MeSH lifesciencedb.jp
Microsatellite Repeats マイクロサテライトリピート MeSH lifesciencedb.jp
Pigmentation 色素沈着 MeSH lifesciencedb.jp
Lod Score ロッドスコア MeSH lifesciencedb.jp
Codon, Nonsense ナンセンスコドン MeSH lifesciencedb.jp
Protein Structure, Tertiary 蛋白質三次構造 MeSH lifesciencedb.jp
Frameshift Mutation フレームシフト変異 MeSH lifesciencedb.jp
Apoptosis アポトーシス MeSH lifesciencedb.jp
Gene Expression 遺伝子発現 MeSH lifesciencedb.jp
Haplotypes ハプロタイプ MeSH lifesciencedb.jp
Mutation 変異 MeSH lifesciencedb.jp
Follow-Up Studies 追跡研究 MeSH lifesciencedb.jp
Amino Acid Sequence アミノ酸配列 MeSH lifesciencedb.jp
Base Sequence 塩基配列 MeSH lifesciencedb.jp



Anatomy

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MeSH term Japanese Link 01
Chromosomes, Human, Pair 17 ヒト第17染色体 MeSH lifesciencedb.jp
Sweat Glands 汗腺 MeSH lifesciencedb.jp



Organisms

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MeSH term Japanese Link 01
Humans ヒト MeSH lifesciencedb.jp



Database Center for Life Science