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  • nodular lymphosarcoma
    °áÀý¼º ¸²ÇÁ À°Á¾
  • nodular melanoma
    °áÀý¼º Èæ»öÁ¾(~ýÙßäðþ)
  • nodular mesoneuritis
    °áÀý¼º ½Å°æÃʳ»¿°(~ãêÌèõªÒ®æú).
  • nodular mycosis fungoides
    °áÀý¼º±Õ»ó ½ÄÀ°Á¾
  • nodular myolysis
    °áÀý¼º ±Ùº¯¼º(~ÐÉܨàõ).
  • nodular nonsuppurative panniculitis
    °áÀý»óºñÈ­³ó¼º ÇÇÇÏÁö¹æÃþ¿°(Ì¿ï½ßÒÞª ûùÒÛàõù«ù»ò·Û¸öµæú)
  • nodular nonsuppurative panniculitis
    °áÀý»óºñÈ­³ó¼º ÇÇÇÏÁö¹æÃþ¿°(¡­ßÒÞªûùÒÛàõù«ù»ò·Û¸öµæú)
  • nodular nontoxic goiter
    °áÀýºñÁßµ¶¼º °©»ó¼±Á¾(Ì¿ï½ÞªñéÔ¸àõË£ßÒàÍðþ).
  • nodular nontoxic goiter
    °áÀýºñÁßµ¶¼º °©»ó¼±Á¾(¡­ÞªñéÔ¸àõË£ßÒàÍðþ)
  • nodular nontoxic goiter
    °áÀý¼ººñÁßµ¶¼º °©»ó¼±Á¾(°áÀý¼ººñÁßµ¶¼º°©»ó¼±Á¾).
  • nodular panniculitis
    °áÀý¼º Áö¹æ¿°(¡­ò·Û¸æú)
  • nodular pattern
    ¼Ò°áÀý ¾ç»ó
  • nodular prurigo ³ª prurigo nodularis
    °áÀý¼º ¾çÁø(~åÊòÖ)
  • nodular pseudosarcomatous fasciitis
    °áÀý¼º °¡¼º À°Á¾¼º ±Ù¸·¿°
  • nodular salpingitis
    °áÀý¼º ³­°ü¿°(~հηæú).
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ALD Adreno-Leuko-Dystrophy
APECED Autoimmune Poly-Endocrinopathy Candidiasis Ectodermal Dystrophy
DMD Duchenne type Muscular Dystrophy; ¾Ç¼ºÇü DuchenneÇü ±ÙÀÌ¿µ¾çÁõ
MLD Metachromatic Leuko-Dystrophy
RSDS Reflex Sympathetic Dystrophy Syndrome
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NAD Neuroaxonal dystrophy
OPMD Oculopharyngeal muscular dystrophy
RSD Reflex Sympathetic Dystrophy
RSDS Reflex Sympathetic Dystrophy Syndrome
SCARMD Severe childhood autosomal recessive muscular dystrophy
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Leyden-Mobius muscular dystrophy One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance.
Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy.
(05 Mar 2000)
limb-girdle muscular dystrophy One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance.
Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy.
(05 Mar 2000)
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