G12.1 – Other inherited spinal muscular atrophy
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Applicable To
Adult form spinal muscular atrophy
Childhood form, type II spinal muscular atrophy
Distal spinal muscular atrophy
Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]
Progressive bulbar palsy of childhood [Fazio-Londe]
Scapuloperoneal form spinal muscular atrophy
GEM Conversion to ICD-9 CM
Fs: 10000
–
Kugelberg-Welander disease
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Atrophy, atrophic
(of)
muscle, muscular
(diffuse) (general) (idiopathic) (primary)
M62.50
progressive
(bulbar)
G12.21
juvenile form, type III
(Kugelberg- Welander)
G12.1
of childhood
(Fazio-Londe)
G12.1
Sibling Codes
Parent Sibling Codes
View in Tabular
Code | Title |
---|---|
G00-G99 | Diseases of the nervous system (G00-G99) |
G10-G14 | Systemic atrophies primarily affecting the central nervous system (G10-G14) |
G12 | Spinal muscular atrophy and related syndromes |
G12.1 |
Other inherited spinal muscular atrophy
Applicable to
Adult form spinal muscular atrophy
Childhood form, type II spinal muscular atrophy
Distal spinal muscular atrophy
Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]
Progressive bulbar palsy of childhood [Fazio-Londe]
Scapuloperoneal form spinal muscular atrophy
|