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G711 Áõ»ó¼º ±Ù±äÀåÁõ Symptomatic myotonia
G711 ¼±Ãµ¼º ±Ù±äÀåÁõNOS Myotonia congenita NOS
G711 ¿ì¼º[Åè½¼] ¼±Ãµ¼º ±Ù±äÀåÁõ Dominant[Thomsen] myotonia congenital
G711 ¿­¼º[º£Ä¿] ¼±Ãµ¼º ±Ù±äÀåÁõ Recessive[Becker] myotonia congenital
G711 ½Å°æ±Ù±äÀåÁõ[¾ÆÀÌÀÛ½º] Neuromyotonia[Isaacs]
G711 ¼±Ãµ¼º ÀÌ»ó±Ù±äÀåÁõ Paramyotonia congenital
G711 °ÅÁþ±Ù±äÀåÁõ Pseudomyotonia
G712 ¼±Ãµ¼º ±Ùº´Áõ Congenital myopathies
G712 ¼±Ãµ¼º ±Ùµð½ºÆ®·ÎÇÇ NOS Congenital muscular dystrophy NOS
G712 ±Ù¼¶À¯ÀÇ Æ¯ÀÌÀû ÇüÅÂÀû ÀÌ»óÀ» µ¿¹ÝÇÑ ¼±Ãµ¼º ±Ùµð½ºÆ®·ÎÇÇ Congenital muscular dystrophy with specific morphological abnormalities of the muscle fibre
G712 Áß½ÉÇÙ º´ Central core disease
G712 ¹Ì¼¼ÇÙ º´ Minicore disease
G712 ´Ù¹ß½É º´ Multicore disease
G712 ±Ù¼¶À¯Çü ºÒ±ÕÇü Fibre-type disproportion
G712 ±Ù¼¼°ü¼º(Áß½ÉÇÙ¼º) ±Ùº´Áõ Myotubular(centronluclear) myopathy
G712 ³×¸»¸°±Ùº´Áõ Nemaline myopathy
G713 ´Þ¸® ºÐ·ùµÇÁö ¾ÊÀº ¹ÌÅäÄܵ帮¾Æ±Ùº´Áõ Mitochondrial myopathy, NEC
G718 ±âŸ ±ÙÀ°ÀÇ ÀÏÂ÷¼º Àå¾Ö Other primary disorders of muscles
G719 »ó¼¼ºÒ¸íÀÇ ±ÙÀ°ÀÇ ÀÏÂ÷¼º Àå¾Ö Primary disorder of muscle, unspecified
G719 À¯Àü¼º ±Ùº´Áõ NOS Hereditary myopathy NOS
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