Alphabetic Index · main term
Déjérine-Sottas disease or neuropathy (hypertrophic)
Déjérine-Sottas disease or neuropathy (hypertrophic) is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists G60.0 for this term: Hereditary motor and sensory neuropathy. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Hereditary motor and sensory neuropathy
Other Index terms that lead to G60.0
Different words, same code. 22 entries
- Ataxia, ataxy, ataxic, Roussy-Lévy
- Atrophy, atrophic (of), Charcot-Marie-Tooth
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), neuropathic (peroneal) (progressive)
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), peroneal
- Charcot-Marie-Tooth disease, paralysis or syndrome
- Curvature, spine (acquired) (angular) (idiopathic) (incorrect) (postural), due to or associated with, Charcot-Marie-Tooth disease
- Dystrophy, dystrophia, muscular, progressive (hereditary), Charcot-Marie (-Tooth) type
- Marie-Charcot-Tooth neuropathic muscular atrophy
- Neuritis (rheumatoid), Déjérine-Sottas
- Neuritis (rheumatoid), interstitial hypertrophic progressive
- Neuritis (rheumatoid), progressive hypertrophic interstitial
- Neuropathy, neuropathic, Déjérine-Sottas
Show 10 more
- Neuropathy, neuropathic, hereditary, motor and sensory (types I-IV)
- Neuropathy, neuropathic, hypertrophic
- Neuropathy, neuropathic, hypertrophic, Charcot-Marie-Tooth
- Neuropathy, neuropathic, hypertrophic, Déjérine-Sottas
- Neuropathy, neuropathic, hypertrophic, interstitial progressive
- Neuropathy, neuropathic, hypertrophic, of infancy
- Neuropathy, neuropathic, motor and sensory, hereditary (types I-IV)
- Neuropathy, neuropathic, progressive, hypertrophic interstitial
- Paralysis, paralytic (complete) (incomplete), Charcot-Marie-Tooth type
- Roussy-Lévy syndrome