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01	136520	-	FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROME	-

Disease

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	MeSH term	Japanese	Link	01
	Nystagmus, Pathologic	眼振
	Eye Abnormalities	眼奇形
	Vision Disorders	視覚障害
	Cataract	白内障
	Nystagmus, Congenital	先天性眼振
	Ectopia Lentis	水晶体偏位
	Aniridia	無虹彩
	Corneal Diseases	角膜疾患
	Macular Degeneration	網膜黄斑変性
	Syndrome	症候群

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Chemicals

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	MeSH term	Japanese	Link	01
	Paired Box Transcription Factors	Paired Box Transcription Factors
	Eye Proteins	眼球蛋白質
	Homeodomain Proteins	ホメオドメイン蛋白質
	Repressor Proteins	レプレッサー蛋白質
	DNA-Binding Proteins	DNA結合タンパク
	RNA Splice Sites	RNAスプライス部位
	Transcription Factors	転写因子
	RNA, Messenger	メッセンジャーRNA

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Biological Phenomena

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	MeSH term	Japanese	Link	01
	Visual Acuity	視力
	Polymorphism, Single-Stranded Conformational	PCR-SSCP法
	Amino Acid Sequence	アミノ酸配列
	RNA Splice Sites	RNAスプライス部位
	Binding Sites	結合部位
	Amino Acid Substitution	アミノ酸置換
	Sequence Homology, Amino Acid	アミノ酸配列相同性
	Base Sequence	塩基配列
	Mutation, Missense	ミスセンス変異
	Point Mutation	点変異
	Genes, Dominant	優性遺伝子
	Phenotype	表現型
	Mutation	変異

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Anatomy

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	MeSH term	Japanese	Link	01
	Fovea Centralis	中心窩
	Macula Lutea	黄斑
	Iris	虹彩
	Fundus Oculi	眼底

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Organisms

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	MeSH term	Japanese	Link	01
	Humans	ヒト

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