G588 | ±âŸ ¸í½ÃµÈ ´ÜÀϽŰ溴Áõ | Other specified mononeuropathies |
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G589 | »ó¼¼ºÒ¸íÀÇ ´ÜÀϽŰ溴Áõ | Mononeuropathy, unspecified |
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G59 | ´Þ¸® ºÐ·ùµÈ Áúȯ¿¡¼ÀÇ ´ÜÀϽŰ溴Áõ | Mononeuropathy in diseases classified elsewhere |
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G590 | ´ç´¢º´¼º ´Ü¹ß ½Å°æº´Áõ (4´ÜÀ§ ¼ýÀÚ .4¿¡ ÇØ´çµÇ´Â E10-E14+) | Diabetic mononeuropathy (E10-E14+ ¿¡¼ .4) |
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G598 | ´Þ¸® ºÐ·ùµÈ Áúȯ¿¡¼ÀÇ ±âŸ ´ÜÀϽŰ溴Áõ | Other mononeuropathies in diseases classified elsewhere |
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G60 | À¯Àü¼º ¹× Ư¹ß¼º ½Å°æº´Áõ | Hereditary and idiopathic neuropathy |
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G600 | À¯Àü¼º ¿îµ¿ ¹× °¨°¢ ½Å°æº´Áõ | Hereditary motor and sensory neuropathy,types |
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G600 | »þ¸£ÄÚ-¸¶¸®-Åõ½ºº´ | Charcot-Marie-Tooth disease |
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G600 | µ¥Á¦¸°-¼ÒŸ½ºº´ | Dejerine-Sottas disease |
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G600 | À¯Àü¼º ¿îµ¿ ¹× °¨°¢ ½Å°æº´Áõ I-¥³Çü | Hereditary motor and sensory neuropathy,types ¥°-¥³ |
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G600 | ¿µ¾Æ±âÀÇ ºñ´ë¼º ½Å°æº´Áõ | Hypertrophic neuropathy of infancy |
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G600 | ºñ°ñ±ÙÀ§Ãà(Ãà»èÇü, ºñ´ëÇü) | Peroneal muscular atrophy (axonal type, hypertrophic type) |
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G600 | ·ç½Ã-·¹ºñÁõÈıº | Roussy-Levy syndrome |
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G601 | ·¹ÇÁ¼¶º´ | Refsum's disease |
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G602 | À¯Àü¼º ¿îµ¿½ÇÁ¶¿Í ¿¬°üµÈ ½Å°æº´Áõ | Neuropathy in association with hereditary ataxia |
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G603 | Ư¹ß¼º ÁøÇ༺ ½Å°æº´Áõ | Idiopathic progressive neuropathy |
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G608 | ±âŸ À¯Àü¼º ¹× Ư¹ß¼º ½Å°æº´Áõ | Other hereditary and idiopathic neuropathies |
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G608 | ¸ð¸£¹Ýº´ | Morvan's disease |
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G608 | ³Ú¶óÅæÁõÈıº | Nelaton's syndrome |
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G608 | ¿ì¼º À¯Àü°¨°¢½Å°æº´Áõ | Dominantly inherited sensory neuropathy |
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