OMIM → Related disease, drugs, ...
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01
604185
HCFP2
FACIAL PARESIS, HEREDITARY, CONGENITAL
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Disease
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Chemicals
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Biological Phenomena
:
Anatomy
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Organisms
Disease
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MeSH term
Japanese
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01
Facial Paralysis
顔面麻痺
Hearing Disorders
聴力障害
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
Penetrance
浸透度(遺伝学)
Chromosomes, Human, Pair 10
ヒト第10染色体
Recombination, Genetic
遺伝子組換え
Chromosomes, Human, Pair 3
ヒト第3染色体
Genetic Heterogeneity
遺伝的異質性
Heterozygote
ヘテロ接合体
Polymorphism, Genetic
遺伝子多型
Haplotypes
ハプロタイプ
Genetic Markers
遺伝子マーカー
Phenotype
表現型
Lod Score
ロッドスコア
Genes, Dominant
優性遺伝子
Genetic Linkage
連鎖(遺伝学)
Anatomy
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MeSH term
Japanese
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01
Chromosomes, Human, Pair 10
ヒト第10染色体
Chromosomes, Human, Pair 3
ヒト第3染色体
Organisms
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MeSH term
Japanese
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01
Humans
ヒト
Database Center for Life Science