G08 | µÎ°³°³» ¶Ç´Â ôÃß³» Á¤¸Æµ¿ ¹× Á¤¸ÆÀÇ ÆÐÇ÷¼º Ç÷ÀüÁõ | Septic embolism of intracranial or intraspinal veous sinuses and veins |
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G09 | ÁßÃ߽Űæ°èÅëÀÇ ¿°Áõ¼º ÁúȯÀÇ ÈÄÀ¯Áõ | Sequelae of inflammatory diseases of central nervous system |
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G10 | ÇåÆÃÅ溴 | Huntington's disease |
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G10 | ÇåÆÃÅ湫µµº´ | Huntington's chorea |
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G11 | À¯Àü¼º ¿îµ¿½ÇÁ¶ | Hereditary ataxia |
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G110 | ¼±Ãµ¼º ºñÁøÇ༺ ¿îµ¿½ÇÁ¶ | Congenital nonprogressive ataxia |
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G111 | Á¶±â¹ßº´ ¼Ò³ú¼º ¿îµ¿½ÇÁ¶ | Early-onset cerebellar ataxia |
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G111 | º»Å¼º ¶³¸²À» µ¿¹ÝÇÑ Á¶±â¹ßº´ ¼Ò³ú¼º ¿îµ¿½ÇÁ¶ | Early-onset cerebellar ataxia with essential tremer |
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G111 | ¸¶ÀÌ¿ÀŬ·Î´©½º[ÇåÆ®¿îµ¿½ÇÁ¶]¸¦ µ¿¹ÝÇÑ Á¶±â¹ßº´ ¼Ò³ú¼º ¿îµ¿½ÇÁ¶ | Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia] |
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G111 | º¸·ùµÈ °Ç¹Ý»ç¸¦ µ¿¹ÝÇÑ Á¶±â¹ßº´ ¼Ò³ú¼º ¿îµ¿½ÇÁ¶ | Early-onset cerebellar ataxia with retained tendon reflexes |
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G111 | ÇÁ¸®µå¶óÀÌÈ÷¿îµ¿½ÇÁ¶(º¸Åë¿°»öü¿¼º) | Friedreich's ataxia (autosomal recessive) |
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G111 | X-¿¬°ü ¿¼º ô¼ö¼Ò³ú¼º ¿îµ¿½ÇÁ¶ | X-linked recessive spinocerebellar ataxia |
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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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