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01
302380
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CATEL-MANZKE 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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MeSH term
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01
Pierre Robin Syndrome
Pierre Robin症候群
Heart Defects, Congenital
心臓疾患-先天性
Syndrome
症候群
Micrognathism
小顎症
Abnormalities, Multiple
奇形-多発
Bone Diseases, Developmental
骨発育異常
Hand Deformities, Congenital
手の形態異常-先天性
Funnel Chest
漏斗胸
Cleft Palate
口蓋裂
Dislocations
脱臼
Foot Deformities, Congenital
足の形態異常-先天性
Growth Disorders
成長障害
Chemicals
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MeSH term
Japanese
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01
Genetic Markers
遺伝子マーカー
Biological Phenomena
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MeSH term
Japanese
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01
X Chromosome
X染色体
Genetic Markers
遺伝子マーカー
Genetic Linkage
連鎖(遺伝学)
Phenotype
表現型
Anatomy
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MeSH term
Japanese
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01
Fingers
手指
Metacarpus
中手骨
X Chromosome
X染色体
Toes
足指
Knee Joint
膝関節
Face
顔面
Bone and Bones
骨
Organisms
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MeSH term
Japanese
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01
Humans
ヒト
Database Center for Life Science