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01
608591
CMT2G
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2G
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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
Foot Deformities, Acquired
足の形態異常-後天性
Nerve Degeneration
神経変性
Hereditary Sensory and Autonomic Neuropathies
遺伝性感覚自律性ニューロパシー
Peripheral Nervous System Diseases
末梢神経系疾患
Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth病
Muscular Atrophy
筋萎縮症
Chemicals
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MeSH term
Japanese
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01
Biological Phenomena
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MeSH term
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01
Locomotion
移動運動
Neural Conduction
神経興奮伝導
Chromosomes, Human, Pair 12
ヒト第12染色体
Age of Onset
発病年齢
Haplotypes
ハプロタイプ
Lod Score
ロッドスコア
Genes, Dominant
優性遺伝子
Anatomy
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MeSH term
Japanese
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01
Ganglia, Spinal
脊髄神経節
Peripheral Nerves
末梢神経
Chromosomes, Human, Pair 12
ヒト第12染色体
Organisms
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MeSH term
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01
Humans
ヒト
Database Center for Life Science