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692222
OPA5
optic atrophy 5 (autosomal dominant)
Disease
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Chemicals
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Biological Phenomena
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Organisms
Disease
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5
Optic Atrophy, Autosomal Dominant
視神経萎縮-遺伝性-常染色体優性
Optic Atrophy, Hereditary, Leber
視神経萎縮-遺伝性-Leber
Chemicals
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MeSH term
Japanese
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P
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5
GTP Phosphohydrolases
グアノシン三リン酸ホスホヒドロラーゼ
Biological Phenomena
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MeSH term
Japanese
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O
P
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5
Chromosomes, Human, Pair 22
ヒト第22染色体
Chromosomes, Human, Pair 3
ヒト第3染色体
Mutation
変異
Anatomy
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MeSH term
Japanese
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5
Chromosomes, Human, Pair 22
ヒト第22染色体
Mitochondria
ミトコンドリア
Chromosomes, Human, Pair 3
ヒト第3染色体
Organisms
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MeSH term
Japanese
Link
O
P
A
5
Humans
ヒト