OMIM → Related disease, drugs, ...
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01
600624
CORD1
CONE-ROD DYSTROPHY 1
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Disease
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Chemicals
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Biological Phenomena
:
Anatomy
:
Organisms
Disease
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MeSH term
Japanese
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01
Optic Atrophy, Hereditary, Leber
視神経萎縮-遺伝性-Leber
Retinitis Pigmentosa
網膜色素変性症
Disease Models, Animal
疾患モデル(動物)
Chromosome Deletion
染色体欠失
Intellectual Disability
精神発達遅滞
Abnormalities, Multiple
奇形-多発
Chemicals
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MeSH term
Japanese
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01
Codon, Nonsense
ナンセンスコドン
Proteins
蛋白質
Biological Phenomena
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MeSH term
Japanese
Link
01
Mutagenesis, Insertional
挿入型変異誘発
Codon, Nonsense
ナンセンスコドン
Chromosomes, Human, Pair 14
ヒト第14染色体
Chromosomes, Human, Pair 18
ヒト第18染色体
Exons
エクソン
Chromosome Deletion
染色体欠失
Anatomy
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MeSH term
Japanese
Link
01
Photoreceptor Cells
光受容体
Chromosomes, Human, Pair 14
ヒト第14染色体
Chromosomes, Human, Pair 18
ヒト第18染色体
Organisms
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MeSH term
Japanese
Link
01
Dogs
イヌ
Animals
動物
Humans
ヒト
Database Center for Life Science