G112 | ¸¸±â¹ßº´ ¼Ò³ú¼º ¿îµ¿½ÇÁ¶ | Late-onset cerebellar ataxia |
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G113 | DNA º¹±¸°á¼ÕÀ» ¼ö¹ÝÇÑ ¼Ò³ú¼º ¿îµ¿½ÇÁ¶ | Cerebellar ataxia with defective DNA repair |
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G113 | ¸ð¼¼Ç÷°üÈ®Àå ¿îµ¿½ÇÁ¶[·çÀÌ-¹Ù] | Ataxia telangiectasia[Louis-bar] |
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G114 | À¯Àü¼º °Á÷¼º ÇϹݽŸ¶ºñ | Hereditary spastic paraplegia |
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G118 | ±âŸ À¯Àü¼º ¿îµ¿½ÇÁ¶ | Other hereditary ataxias |
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G119 | »ó¼¼ºÒ¸íÀÇ À¯Àü¼º ¿îµ¿½ÇÁ¶ | Hereditary ataxia, unspecified |
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G119 | À¯Àü¼º ¼Ò³ú¿îµ¿½ÇÁ¶ NOS | Hereditary cerebellar ataxia NOS |
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G119 | À¯Àü¼º ¼Ò³úº¯¼º | Hereditary cerebellar degeneration |
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G119 | À¯Àü¼º ¼Ò³úº´ | Hereditary cerebellar disease |
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G119 | À¯Àü¼º ¼Ò³úÁõÈıº | Hereditary cerebellar syndrome |
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G12 | ô¼ö¼º ±ÙÀ§Ãà ¹× °ü·Ã ÁõÈıº | Spinal muscular atrophy and related syndromes |
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G120 | ¿µ¾ÆÃ´¼ö¼º ±ÙÀ§Ãà, ¥°Çü[º£¸£µå´ÏÈ÷-È£ÇÁ¸¸] | Infantile spinal muscular atrophy, type I[Werdnig-Hoffman] |
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G121 | ±âŸ À¯Àü¼º ô¼ö¼º ±ÙÀ§Ãà | Other inherited spinal muscular atrophy |
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G121 | ¼Ò¾Æ±âÀÇ ÁøÇ༺ ±¸¸¶ºñ [ÆÄÁö¿À-·Ðµ¥] | Progressive bulbar palsy of childhood[Fazio-Londe] |
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G121 | ô¼ö¼º ±ÙÀ§Ãà | Spinal muscular atrophy |
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G121 | ¼ºÀÎÇü ô¼ö¼º ±ÙÀ§Ãà | Adult form spinal muscular atrophy |
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G121 | ¼Ò¾ÆÇü, ¥±Çü ô¼ö¼º ±ÙÀ§Ãà | Childhood form, type ¥±,spinal muscular atrophy |
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G121 | ¿øÀ§¼º ô¼ö¼º ±ÙÀ§Ãà | Distal spinal muscular atrophy |
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G121 | ¿¬¼ÒÇü, ¥²Çü [Äí°Öº£¸£±×-º§¶õ´õ] ô¼ö¼º ±ÙÀ§Ãà | Juvenile form,type¥²[Kugelberg -Welander] spinal muscular atrophy |
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G121 | ¾î±úÁ¾¾Æ¸® Çü ô¼ö¼º ±ÙÀ§Ãà | Scapuloperoneal form spinal muscular atrophy |
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