Myasthenia gravis without (acute) exacerbation Notes: Myasthenia gravis NOS
G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction Notes: Limb girdle muscular dystrophy ty…
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction Notes: Limb girdle muscular dystrophy type 2A ; LGMD R1 calpain-3-related ; Primary calpainopathy
G71.19 Other specified myotonic disorders Notes: Myotonia fluctuans ; Myotonia permanens ; Neuromyotonia [Isaacs] ; Paramyotoni…
Other specified myotonic disorders Notes: Myotonia fluctuans ; Myotonia permanens ; Neuromyotonia ; Paramyotonia congenita (of von Eulenburg) ; Pseudomyotonia ; Symptomatic myotonia
G56.82 Other specified mononeuropathies of left upper limb
Other specified mononeuropathies of left upper limb
G57.12 Meralgia paresthetica, left lower limb
Meralgia paresthetica, left lower limb
G57.43 Lesion of medial popliteal nerve, bilateral lower limbs
Lesion of medial popliteal nerve, bilateral lower limbs
G57.80 Other specified mononeuropathies of unspecified lower limb
Other specified mononeuropathies of unspecified lower limb
G60.0 Hereditary motor and sensory neuropathy Notes: Charcot-Marie-Tooth disease ; Déjérine-Sottas disease ; Hereditary motor …
Hereditary motor and sensory neuropathy Notes: Charcot-Marie-Tooth disease ; Déjérine-Sottas disease ; Hereditary motor and sensory neuropathy, types I-IV ; Hypertrophic neuropathy of infancy ; Perone ...