E79 | Ç»¸° ¹× ÇǸ®¹Ìµò ´ë»çÀå¾Ö | Disorders of purine and pyrimidine metabolism |
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E790 | ¿°Áõ¼º °üÀý¿° ¹× Åëdz¼º ÁúȯÀÇ Â¡ÈÄ°¡ ¾ø´Â °í¿ä»êÇ÷Áõ | Hyperuricemia without signs of inflammatory arthritis and tophaceous disease |
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E790 | ¹«Áõ»ó °í¿ä»êÇ÷Áõ | Asymptomatic hyperuricemia |
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E791 | ·¹½¬-´ÏÇÑÁõÈıº | Lesch-Nyhan syndrome |
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E798 | ±âŸ Ç»¸° ¹× ÇǸ®¹Ìµò ´ë»çÀå¾Ö | Other disorders of purine and pyrimidine metabolism |
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E798 | À¯Àü¼º »êƾ´¢Áõ | Hereditary xanthinuria |
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E799 | »ó¼¼ºÒ¸íÀÇ Ç»¸° ¹× ÇǸ®¹Ìµò ´ë»çÀå¾Ö | Disorder of purine and pyrimidine metabolism, unspecified |
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E80 | Æ÷¸£ÇǸ° ¹× ºô¸®·çºó ´ë»çÀå¾Ö | Disorders of porphyrin and bilirubin metabolism |
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E80 | Ä«Å»·¹À̽º ¹× °ú»êÈÈ¿¼ÒÀÇ °á¼Õ | Defects of catalase and peroxidase |
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E800 | À¯Àü¼º ÀûÇ÷±¸Á¶Ç÷Æ÷¸£ÇǸ°Áõ | Hereditary erythropoietic porphyria |
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E800 | ¼±Ãµ¼º ÀûÇ÷±¸Á¶Ç÷Æ÷¸£ÇǸ°Áõ | Congenital erythropoietic porphyria |
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E800 | ÀûÇ÷±¸Á¶Ç÷ÇÁ·ÎÅäÆ÷¸£ÇǸ°Áõ | Erythropoietic protoporphyria |
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E801 | ¸¸¹ß¼º ÇǺÎÆ÷¸£ÇǸ°Áõ | Porphyria cutanea tarda |
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E802 | ±âŸ Æ÷¸£ÇǸ°Áõ | Other porphyria |
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E802 | À¯Àü¼º ÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ | Hereditary coproporphyria |
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E802 | Æ÷¸£ÇǸ°Áõ NOS | Porphyria NOS |
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E802 | ±Þ¼º °£Ç漺(°£¼º) Æ÷¸£ÇǸ°Áõ | Acute intermittent (hepatic) porphyria |
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E803 | Ä«Å»·¹À̽º ¹× °ú»êÈÈ¿¼ÒÀÇ °á¼Õ | Defects of catalase and peroxidase |
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E803 | ¹«Ä«Å»·¹À̽ºÁõ[Ÿ°¡Ç϶ó] | Acatalasia[Takahara] |
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E804 | Áúº£¸£ÁõÈıº | Gilbert's syndrome |
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