D763 | ½ÉÇÑ ¸²ÇÁÀýº´ÁõÀ» µ¿¹ÝÇÑ µ¿Á¶Á÷±¸Áõ | Sinus histiocytosis with massive lymphadenopathy |
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D763 | Ȳ»öÀ°¾ÆÁ¾ | Xanthogranuloma |
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D77 | ´Þ¸® ºÐ·ùµÈ Áúȯ¿¡¼ Ç÷¾× ¹× Á¶Ç÷±â°üÀÇ ±âŸ Àå¾Ö | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
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D77 | ÁÖÇ÷ÈíÃæÁõ¿¡¼ ºñÀåÀÇ ¼¶À¯Áõ | Fibrosis of spleen in schistosomiasis[bilharziasis] (B65.-+) |
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D80 | Ç×ü°á¼ÕÀÌ ÇöÀúÇÑ ¸é¿ª°áÇÌÁõ | Immunodeficiency with predominantly antibody defects |
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D800 | À¯Àü¼º Àú°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ | Hereditary hypogammaglobulinemia |
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D800 | º¸Åë¿°»öü¿¼º ¹«°¨¸¶±Û·ÎºÒ¸°Ç÷µî(½ºÀ§½ºÇü) | Autosomal recessive agammaglobulinaemia (Swiss type) |
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D800 | X-¿¬°ü ¹«°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ[ºê·çÅæ](¼ºÀåÈ£¸£¸ó°áÇÌÀ» µ¿¹Ý) | X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency) |
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D801 | ºñ°¡Á·¼º Àú°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ | Nonfamilial hypogammaglobulinemia |
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D801 | ¸é¿ª±Û·ÎºÒ¸°À» Áö´Ñ B-¸²ÇÁ±¸°¡ ÀÖ´Â ¹«°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ | Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes |
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D801 | °øÅë°¡º¯¼º ¹«°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ | Commonvariable agammaglobulinaemia [CVA Agamma] |
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D801 | Àú°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ NOS | Hypogammaglobulinaemia NOS |
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D802 | ¸é¿ª±Û·ÎºÒ¸°AÀÇ ¼±ÅÃÀû °áÇÌ | Selective deficiency of immunoglobulin A[lgA] |
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D803 | ¸é¿ª±Û·ÎºÒ¸°G ¼ºêŬ·¡½ºÀÇ ¼±ÅÃÀû °áÇÌ | Selective deficiency of immunoglobulin G[lgG] subclasses |
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D804 | ¸é¿ª±Û·ÎºÒ¸°MÀÇ ¼±ÅÃÀû °áÇÌ | Selective deficiency of immunoglobulin M[lgM] |
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D805 | ¸é¿ª±Û·ÎºÒ¸°MÀÇ Áõ°¡¸¦ µ¿¹ÝÇÑ ¸é¿ª°áÇÌ | Immunodeficiency with increased immunoglobulin M[lgM] |
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D806 | °ÅÀÇ Á¤»óÀÇ ¸é¿ª±Û·ÎºÒ¸° ¶Ç´Â °í¸é¿ª±Û·ÎºÒ¸°Ç÷ÁõÀ» µ¿¹ÝÇÑ Ç×ü°áÇÌ | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
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D807 | ¿µ¾Æ±âÀÇ ÀÏ°ú¼º Àú°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ | Transient hypogammaglobulinemia of infancy |
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D808 | Ç×ü°á¼ÕÀÌ ÇöÀúÇÑ ±âŸ ¸é¿ª°áÇÌ | Other immunodeficiencies with predominantly antibody defects |
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D808 | Ä«ÆÄ°æ¼â°áÇÌ | Kappa light chain deficiency |
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