D552 | ÇÇ·çºê»ê¿° Ä«À̳×À̽º°áÇ̺óÇ÷ | Anemia pyruvate kinase[PK] deficiency |
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D552 | »ïź´çÀλ꿰À̼ºÈÈ¿¼Ò °áÇ̼º ºóÇ÷ | Anemia triose-phosphate isomerase deficiency |
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D553 | ´ºÅ¬·¹¿ÀŸÀÌµå ´ë»çÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to disorders of nucleotide metabolism |
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D558 | ±âŸ È¿¼ÒÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Other anemias due to enzyme disorders |
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D559 | »ó¼¼ºÒ¸íÀÇ È¿¼ÒÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to enzyme disorder, unspecified |
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D56 | ÁöÁßÇØºóÇ÷ | Thalassemia |
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D560 | ¾ËÆÄ ÁöÁßÇØºóÇ÷ | Alpha thalassemia |
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D561 | º£Å¸ ÁöÁßÇØºóÇ÷ | Beta thalassaemia |
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D561 | Äí¿ï¸®ºóÇ÷ | Cooley's anemia |
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D561 | ÁßÁõ º£Å¸ÁöÁßÇØºóÇ÷ | Severe beta thalassaemia |
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D561 | Áß°£Çü ÁöÁßÇØºóÇ÷ | Intermedia thalassaemia |
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D561 | ÁßÁõ ÁöÁßÇØºóÇ÷ | Major thalassaemia |
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D562 | µ¨Å¸-º£Å¸ ÁöÁßÇØºóÇ÷ | Delta-beta thalassemia |
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D563 | ÁöÁßÇØºóÇ÷¼ÒÁú | Thalassemia trait |
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D564 | ÅÂ¾Æ Çì¸ð±Û·ÎºóÀÇ À¯ÀüÀû Á¸¼Ó | Hereditary persistence of fetal hemoglobin [HPFH] |
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D568 | ±âŸ ÁöÁßÇØºóÇ÷ | Other thalassemias |
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D569 | »ó¼¼ºÒ¸íÀÇ ÁöÁßÇØºóÇ÷ | Thalassemia, unspecified |
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D569 | ÁöÁßÇØºóÇ÷(±âŸ Çì¸ð±Û·Îºóº´ÁõÀ» µ¿¹ÝÇÑ) | Mediterrane anemia (with other haemoglobinopathy) |
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D569 | ÁöÁßÇØºóÇ÷(°æÁõÇü, È¥ÇÕÇü, ±âŸ Çì¸ð±Û·Îºóº´ÁõÀ» µ¿¹ÝÇÑ) | Thalassaemia(minor, mixed, with other haemoglobinopathy) |
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D57 | ³´ÀûÇ÷±¸Àå¾Ö | Sickle-cell disorders |
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