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 |
 |