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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G122 | ¿îµ¿´º·±Áúȯ | Motor neuron disease |
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G1220 | °¡Á·¼º ¿îµ¿´º·±Áúȯ | Familial motor neuron disease |
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G1221 | ±ÙÀ§Ã༺ Ãø»è°æÈÁõ | Amyotrophic lateral sclerosis |
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G1222 | ÀÏÂ÷¼º Ãø»è°æÈÁõ | Primary lateral sclerosis |
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G1223 | ÁøÇ༺ ±¸¸¶ºñ | Progressive bulbar palsy |
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G1224 | ÁøÇ༺ ô¼ö¼º ±ÙÀ§Ãà | Progressive spinal muscular atrophy |
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G1228 | ±âŸ ¹× »ó¼¼ºÒ¸íÀÇ ¿îµ¿´º·±Áúȯ | Other and unspecified motor neuron disease |
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G128 | ±âŸ ô¼ö¼º ±ÙÀ§Ãà ¹× °ü·Ã ÁõÈıº | Other spinal muscular atrophies and related syndromes |
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