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01
600886
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HYPERFERRITINEMIA-CATARACT 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
Japanese
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01
Cataract
白内障
Hemochromatosis
ヘモクロマトーシス
Anemia
貧血
Syndrome
症候群
Iron Metabolism Disorders
鉄代謝障害
Eye Diseases, Hereditary
眼疾患-遺伝性
Hematologic Diseases
血液疾患
Nervous System Diseases
神経系疾患
Metabolism, Inborn Errors
代謝異常-先天性
Disease Progression
病勢悪化
Chemicals
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MeSH term
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01
Ferritins
フェリチン
Iron-Regulatory Proteins
鉄調節蛋白質
Apoferritins
アポフェリチン
Iron
鉄
RNA-Binding Proteins
RNA結合タンパク質
Codon, Initiator
開始コドン
Iron-Sulfur Proteins
鉄-硫黄蛋白質
Cation Transport Proteins
カチオン輸送蛋白質
Histocompatibility Antigens Class I
組織適合抗原I
RNA, Messenger
メッセンジャーRNA
HLA Antigens
HLA抗原
Membrane Proteins
膜蛋白質
Biological Phenomena
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MeSH term
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01
Chromosomes, Human, Pair 19
ヒト第19染色体
Point Mutation
点変異
Genes, Dominant
優性遺伝子
Codon, Initiator
開始コドン
Nucleic Acid Conformation
核酸高次構造
Mutation
変異
Base Sequence
塩基配列
Prevalence
有病率
Age of Onset
発病年齢
Follow-Up Studies
追跡研究
Anatomy
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MeSH term
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01
Chromosomes, Human, Pair 19
ヒト第19染色体
Lens, Crystalline
水晶体
Liver
肝臓
Lymphocytes
リンパ球
Cells, Cultured
培養細胞
Organisms
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MeSH term
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01
Humans
ヒト
Database Center for Life Science