D572 | Çì¸ð±Û·Îºó-SCº´ | Hb-SC disease |
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D572 | Çì¸ð±Û·Îºó-SDº´ | Hb-SD disease |
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D572 | Çì¸ð±Û·Îºó-SEº´ | Hb-SE disease |
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D573 | ³´ÀûÇ÷±¸¼ÒÁú | Sickle-cell trait |
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D573 | Çì¸ð±Û·ÎºóS ¼ÒÁú | Hb-S trait |
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D573 | ÀÌÇüÁ¢ÇÕüÇì¸ð±Û·ÎºóS[HbAS] | Heterozygous haemoglobin S |
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D578 | ±âŸ ³´ÀûÇ÷±¸ Àå¾Ö | Other sickle-cell disorders |
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D58 | ±âŸ À¯Àü¼º ¿ëÇ÷¼º ºóÇ÷ | Other hereditary hemolytic anemias |
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D580 | À¯Àü¼º ±¸»óÀûÇ÷±¸Áõ | Hereditary spherocytosis |
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D580 | ¹«´ãÁó´¢¼º(°¡Á·¼º) Ȳ´Þ | Acholuric (familial) jaundice |
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D580 | ¼±Ãµ¼º(±¸»óÀûÇ÷±¸¼º)¿ëÇ÷¼º Ȳ´Þ | Congenital (spherocytic) haemolytic icterus |
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D580 | ¹ÎÄں꽺Ű-¼îÆĵå ÁõÈıº | Minkowski-Chauffard syndrome |
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D581 | À¯Àü¼º Ÿ¿øÇüÀûÇ÷±¸Áõ | Hereditary elliptocytosis |
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D581 | Ÿ¿øÇüÀûÇ÷±¸Áõ(¼±Ãµ¼º) | Elliptocytosis (congenital) |
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D581 | ³ÇüÀûÇ÷±¸Áõ(¼±Ãµ¼º,À¯Àü¼º) | Ovalocytosis, congenital, hereditary |
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D582 | ±âŸ Çì¸ð±Û·Îºóº´Áõ | Other hemoglobinopathies |
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D582 | ÀÌ»óÇì¸ð±Û·Îºó NOS | Abnormal haemoglobin NOS |
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D582 | ¼±Ãµ¼º ÇÏÀÎÃ÷¼ÒüºóÇ÷ | Congenital Heinz body anemia |
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D582 | Çì¸ð±Û·ÎºóCº´ | Hb-C disease |
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D582 | Çì¸ð±Û·ÎºóDº´ | Hb-D disease |
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