E760 | »þÀÌ¿¡ÁõÈıº | Scheie syndrome |
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E761 | II Çü Á¡¾×´Ù´ç·ùÁõ | Mucopolysaccharidosis, type II |
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E761 | ÇåÅÍÁõÈıº | Hunter's syndrome |
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E762 | ±âŸ Á¡¾×´Ù´ç·ùÁõ | Other mucopolysaccharidoses |
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E762 | º£Å¸-±Û·çÅ¥·Î´Ïµ¥À̽º°áÇÌ | ¥â-Glucuronidase deficiency |
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E762 | ¥²,¥³,¥µ,¥¶Çü Á¡¾×´Ù´ç·ùÁõ | Mucopolysaccharidosis,types ¥²,¥³,¥µ,¥¶ |
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E762 | ¸¶·ÎÅä-¶ó¹Ì(°æµµ, ÁßÁõ) ÁõÈıº | Maroteaux-Lamy syndrome(mild, severe) |
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E762 | ¸ð¸£Å°¿À(-À¯»ç)(°íÀüÀû) ÁõÈıº | Morquio syndrome (-like, classic) |
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E762 | »êÇʸ³Æ÷(B,C,DÇü) ÁõÈıº | Sanfilippo (types B,C,D)syndrome |
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E763 | »ó¼¼ºÒ¸íÀÇ Á¡¾×´Ù´ç·ùÁõ | Mucopolysaccharidosis, unspecified |
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E768 | ±âŸ ±Û·çÄÚ»ç¹Ì³ë±Û¶óÀÌÄ´ë»çÀå¾Ö | Other disorders of glucosaminoglycan metabolism |
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E769 | »ó¼¼ºÒ¸íÀÇ ±Û·çÄÚ½º»ç³ë±Û¶óÀÌÄ´ë»çÀå¾Ö | Disorders of glucosaminoglycan metabolism, unspecified |
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E77 | ´ç´Ü¹éÁú´ë»çÀå¾Ö | Disorders of glycoprotein metabolism |
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E770 | ¶óÀ̼ҼØÈ¿¼ÒÀÇ Çؼ®Èĺ¯Á¶ÀÇ °á¼Õ | Defects in post-translational modification of lysosomal enzymes |
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E770 | ¹ÂÄÚÁöÁúÁõ II [I-¼¼Æ÷ º´] | Mucolipidosis ¥± [¥°-cell disease] |
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E770 | ¹ÂÄÚÁöÁúÁõ III[°ÅÁþÇæ·¯ ´Ù¹ßµð½ºÆ®·ÎÇÇ] | Mucolipisosis ¥²[Pseudo-Hurler polydystrophy] |
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E771 | ´ç´Ü¹éÁú ºÐÇØÀÇ°á¼Õ | Defects in glycoprotein degradation |
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E771 | ¾Æ½ºÆĸ£Æ¿±Û·çÄÚ»ç¹Î´¢ | Aspartylglucosaminuria |
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E771 | ǪÄÚ»çÀ̵åÃàÀûÁõ | Fucosidosis |
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E771 | ¸¸³ë»çÀ̵åÃàÀûÁõ | Mannosidosis |
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