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01 604841 STL2 STICKLER SYNDROME, TYPE II - OMIM


Disease : Chemicals : Biological Phenomena : Anatomy : Organisms

Disease

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MeSH term Japanese Link 01
Hearing Loss, Sensorineural 難聴-内耳性 MeSH lifesciencedb.jp
Abnormalities, Multiple 奇形-多発 MeSH lifesciencedb.jp
Connective Tissue Diseases 結合組織疾患 MeSH lifesciencedb.jp
Syndrome 症候群 MeSH lifesciencedb.jp
Esotropia 内斜視 MeSH lifesciencedb.jp
Osteochondrodysplasias 骨軟骨形成異常症 MeSH lifesciencedb.jp
Malocclusion 不正咬合 MeSH lifesciencedb.jp
Eye Diseases, Hereditary 眼疾患-遺伝性 MeSH lifesciencedb.jp
Anodontia 無歯症 MeSH lifesciencedb.jp
Retinal Detachment 網膜剥離 MeSH lifesciencedb.jp
Myopia 近視 MeSH lifesciencedb.jp
Joint Diseases 関節疾患 MeSH lifesciencedb.jp
Craniofacial Abnormalities 頭蓋顔面奇形 MeSH lifesciencedb.jp
Eye Diseases 眼疾患 MeSH lifesciencedb.jp



Chemicals

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MeSH term Japanese Link 01
Collagen Type XI コラーゲンXI型 MeSH lifesciencedb.jp
Collagen 膠原 MeSH lifesciencedb.jp
Valine バリン MeSH lifesciencedb.jp
Glycine アミノ酢酸 MeSH lifesciencedb.jp



Biological Phenomena

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MeSH term Japanese Link 01
Mutation 変異 MeSH lifesciencedb.jp
RNA Splicing RNAスプライシング MeSH lifesciencedb.jp
Genetic Linkage 連鎖(遺伝学) MeSH lifesciencedb.jp
Cephalometry 頭部計測法 MeSH lifesciencedb.jp
Genome, Human ヒトゲノム MeSH lifesciencedb.jp
Chromosomes, Human, Pair 1 ヒト第1染色体 MeSH lifesciencedb.jp
Introns イントロン MeSH lifesciencedb.jp
Phenotype 表現型 MeSH lifesciencedb.jp
Sequence Deletion 配列欠失 MeSH lifesciencedb.jp
Genetic Variation 遺伝的多様性 MeSH lifesciencedb.jp
Homozygote ホモ接合体 MeSH lifesciencedb.jp
Exons エクソン MeSH lifesciencedb.jp
Genes, Recessive 劣性遺伝子 MeSH lifesciencedb.jp
Amino Acid Sequence アミノ酸配列 MeSH lifesciencedb.jp
Genotype 遺伝子型 MeSH lifesciencedb.jp
Base Sequence 塩基配列 MeSH lifesciencedb.jp



Anatomy

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MeSH term Japanese Link 01
Ear MeSH lifesciencedb.jp
Chromosomes, Human, Pair 1 ヒト第1染色体 MeSH lifesciencedb.jp
Joints 関節 MeSH lifesciencedb.jp
Face 顔面 MeSH lifesciencedb.jp



Organisms

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MeSH term Japanese Link 01
Humans ヒト MeSH lifesciencedb.jp



Database Center for Life Science