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692222 OPA5 optic atrophy 5 (autosomal dominant) Entrez Gene lifesciencedb.jp


Disease : Chemicals : Biological Phenomena : Anatomy : Organisms

Disease

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MeSH term Japanese Link O
P
A
5
Optic Atrophy, Autosomal Dominant 視神経萎縮-遺伝性-常染色体優性 MeSH lifesciencedb.jp
Optic Atrophy, Hereditary, Leber 視神経萎縮-遺伝性-Leber MeSH lifesciencedb.jp



Chemicals

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MeSH term Japanese Link O
P
A
5
GTP Phosphohydrolases グアノシン三リン酸ホスホヒドロラーゼ MeSH lifesciencedb.jp



Biological Phenomena

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MeSH term Japanese Link O
P
A
5
Chromosomes, Human, Pair 22 ヒト第22染色体 MeSH lifesciencedb.jp
Chromosomes, Human, Pair 3 ヒト第3染色体 MeSH lifesciencedb.jp
Mutation 変異 MeSH lifesciencedb.jp



Anatomy

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MeSH term Japanese Link O
P
A
5
Chromosomes, Human, Pair 22 ヒト第22染色体 MeSH lifesciencedb.jp
Mitochondria ミトコンドリア MeSH lifesciencedb.jp
Chromosomes, Human, Pair 3 ヒト第3染色体 MeSH lifesciencedb.jp



Organisms

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MeSH term Japanese Link O
P
A
5
Humans ヒト MeSH lifesciencedb.jp