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01
179613
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RECOMBINANT CHROMOSOME 8 SYNDROME
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Disease
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Chemicals
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Biological Phenomena
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Anatomy
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Organisms
Disease
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01
Chromosome Inversion
染色体逆位
Chromosome Aberrations
染色体異常
Syndrome
症候群
Chromosome Disorders
染色体疾患
Tetralogy of Fallot
Fallot四徴症
Chromosome Breakage
染色体切断
Abnormalities, Multiple
奇形-多発
Fetal Diseases
胎児疾患
Chemicals
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01
Biological Phenomena
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MeSH term
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01
Chromosome Inversion
染色体逆位
Chromosomes, Human, Pair 8
ヒト第8染色体
Recombination, Genetic
遺伝子組換え
Chromosome Aberrations
染色体異常
Long Interspersed Nucleotide Elements
広範囲散在反復配列
Terminal Repeat Sequences
末端反復配列
Alu Elements
Alu配列
Chromosome Breakage
染色体切断
Chromosomes, Human, 6-12 and X
ヒト第6-12およびX染色体
Prospective Studies
前向き研究
Heterozygote
ヘテロ接合体
Pregnancy
妊娠
Retrospective Studies
後向き研究
Risk Factors
危険因子
Base Sequence
塩基配列
Phenotype
表現型
Anatomy
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MeSH term
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01
Chromosomes, Human, Pair 8
ヒト第8染色体
Chromosomes, Human, 6-12 and X
ヒト第6-12およびX染色体
Fetus
胎児
Cell Line
細胞系
Organisms
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01
Cricetinae
ハムスター類
Animals
動物
Humans
ヒト
Database Center for Life Science