| cw |
ヒト, ﾋﾄ, human(primates), 012150, human, ポルフィリン症, ﾎﾟﾙﾌｨﾘﾝｼｮｳ, porphyria, 022078, 突然変異, ﾄﾂｾﾞﾝﾍﾝｲ, mutation, 011868, ヘモクロマトーシス, ﾍﾓｸﾛﾏﾄｰｼｽ, hemochromatosis, 057111, * |
| キーワード |
先天性代謝異常, ｾﾝﾃﾝｾｲﾀｲｼｬｲｼﾞｮｳ, inborn errors of metabolism, 054464, *, 先天性疾患, ｾﾝﾃﾝｾｲｼｯｶﾝ, congenital disease, 040292, 病気, ﾋﾞｮｳｷ, disease, 017213, 代謝性疾患, ﾀｲｼｬｾｲｼｯｶﾝ, metabolic disease, 033138, 皮膚病, ﾋﾌﾋﾞｮｳ, skin disease, 012163, 変異, ﾍﾝｲ(ｲﾃﾞﾝ), variation(biology), 012392, ﾍﾝｲ, variation, 先天性金属代謝異常, ｾﾝﾃﾝｾｲｷﾝｿﾞｸﾀｲｼｬｲｼﾞｮｳ, inborn errors of metal metabolism, 057128 |