G60.0 – Hereditary motor and sensory neuropathy
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Applicable To
Charcot-Marie-Tooth disease
Déjérine-Sottas disease
Hereditary motor and sensory neuropathy, types I-IV
Hypertrophic neuropathy of infancy
Peroneal muscular atrophy (axonal type) (hypertrophic type)
Roussy-Levy syndrome
GEM Conversion to ICD-9 CM
Fs: 10000
–
Hereditary peripheral neuropathy
Fs: 10000
–
Peroneal muscular atrophy
Fs: 10000
–
Hereditary sensory neuropathy
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Atrophy, atrophic
(of)
muscle, muscular
(diffuse) (general) (idiopathic) (primary)
M62.50
neuropathic
(peroneal) (progressive)
G60.0
Curvature
spine
(acquired) (angular) (idiopathic) (incorrect) (postural)
See Dorsopathy, deforming
due to or associated with
Déjérine-Sottas disease or neuropathy
(hypertrophic)
G60.0
Dystrophy, dystrophia
progressive
(hereditary)
G71.09
Charcot-Marie type
(-Tooth)
G60.0
motor and sensory
(types I-IV)
G60.0
motor and sensory
See also Polyneuropathy
hereditary
(types I-IV)
G60.0
progressive
Paralysis, paralytic
(complete) (incomplete)
G83.9
Sibling Codes
Parent Sibling Codes
View in Tabular
| Code | Title |
|---|---|
| G00-G99 | Diseases of the nervous system (G00-G99) |
| G60-G65 | Polyneuropathies and other disorders of the peripheral nervous system (G60-G65) |
| G60 | Hereditary and idiopathic neuropathy |
| G60.0 |
Hereditary motor and sensory neuropathy
Applicable to
Charcot-Marie-Tooth disease
Déjérine-Sottas disease
Hereditary motor and sensory neuropathy, types I-IV
Hypertrophic neuropathy of infancy
Peroneal muscular atrophy (axonal type) (hypertrophic type)
Roussy-Levy syndrome
|