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
G56.83 Other specified mononeuropathies of bilateral upper limbs
Other specified mononeuropathies of bilateral upper limbs
G57.13 Meralgia paresthetica, bilateral lower limbs
Meralgia paresthetica, bilateral lower limbs
G57.5 Tarsal tunnel syndrome
Tarsal tunnel syndrome
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 ...
G62.1 Alcoholic polyneuropathy
Alcoholic polyneuropathy