D539 | »ó¼¼ºÒ¸íÀÇ ¿µ¾ç¼º ºóÇ÷ | Nutritional anemia, unspecified |
|
D539 | ´Ü¼ø ¸¸¼º ºóÇ÷ | Simple chronic anemia |
|
D55 | È¿¼ÒÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to enzyme disorders |
|
D550 | Æ÷µµ´ç6ÀÎ »êÅ»¼ö¼ÒÈ¿¼Ò[G6PD] °áÇÌ¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
|
D550 | ÀáµÎÁßµ¶Áõ | Favism |
|
D550 | G6PD °áÇ̺óÇ÷ | G6PD deficiency anemia |
|
D551 | ±âŸ ±Û·çŸƼ¿Â ´ë»çÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to other disorders of glutathione metabolism |
|
D551 | G6PD¸¦ Á¦¿ÜÇÑ À°Åº´ç´ÜÀλ꿰(HMP)¼ÇÆ®°æ·Î¿Í ¿¬°üµÈ È¿¼ÒÀÇ °áÇÌ¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to enzyme deficiencies, except G6PD, relatated to the hexose monophosphate [HMP] shunt pathway |
|
D551 | ¿ëÇ÷¼º ºñ±¸»óÀûÇ÷±¸(À¯Àü¼º)ºóÇ÷,¥°Çü | Anemia due to haemolytic nonsherocytic(hereditary), type I |
|
D552 | ÇØ´ç È¿¼ÒÀÇ Àå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to disorders of glycolytic enzymes |
|
D552 | ¿ëÇ÷¼º ºñ±¸»óÀûÇ÷±¸(À¯Àü¼º)ºóÇ÷,¥±Çü | Anemia haemolytic nonsperocytic(herediary), type II |
|
D552 | Çí¼ÒÄ«À̳×À̽º°áÇ̺óÇ÷ | Anemia hexokinase deficiency |
|
D552 | ÇÇ·çºê»ê¿° Ä«À̳×À̽º°áÇ̺óÇ÷ | Anemia pyruvate kinase[PK] deficiency |
|
D552 | »ïź´çÀλ꿰À̼ºÈÈ¿¼Ò °áÇ̼º ºóÇ÷ | Anemia triose-phosphate isomerase deficiency |
|
D553 | ´ºÅ¬·¹¿ÀŸÀÌµå ´ë»çÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to disorders of nucleotide metabolism |
|
D558 | ±âŸ È¿¼ÒÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Other anemias due to enzyme disorders |
|
D559 | »ó¼¼ºÒ¸íÀÇ È¿¼ÒÀå¾Ö¿¡ ÀÇÇÑ ºóÇ÷ | Anemia due to enzyme disorder, unspecified |
|
D56 | ÁöÁßÇغóÇ÷ | Thalassemia |
|
D560 | ¾ËÆÄ ÁöÁßÇغóÇ÷ | Alpha thalassemia |
|
D561 | º£Å¸ ÁöÁßÇغóÇ÷ | Beta thalassaemia |
|