ICD-10-CM › G00-G99 › G10-G14 › G12 Spinal muscular atrophy and... › G12.1
G12.1
Other inherited spinal muscular atrophy
ValidICD-10-CM diagnosis code.
Valid for claims with a date of service in the current code year.
What has happened to this code
Every change the publisher made, from 2007 to now. Entries marked draft are from the pre-implementation releases: ICD-10 took effect on 1 October 2015, so nothing before FY2016 was ever valid on a claim.
- FY2007 Added to the draft code set draft Other inherited spinal muscular atrophy
How CDC's index refers to this code
Wording from the official alphabetic index. Much of it appears nowhere in the code description, which is why a search for the everyday phrase so often finds nothing.
- Wasting > muscle NEC
- Myelopathic > muscle atrophy
- Atrophy, atrophic > disuse NEC
- Sclerosis, sclerotic > choroid
- Atrophy, atrophic > myopathic NEC
- Disorder > choroid > degeneration
- Atrophy, atrophic > spinal > muscular
- Degeneration, degenerative > chorioretinal
- Degeneration, degenerative > Bruch's membrane
- Atrophy, atrophic > muscle, muscular > myelopathic
- Kugelberg-Welander disease
- Palsy > bulbar > of childhood
- Fazio-Londe disease or syndrome
- Atrophy, atrophic > muscle, muscular > spinal > distal
- Atrophy, atrophic > muscle, muscular > progressive > adult
- Atrophy, atrophic > muscle, muscular > spinal > adult form
- Atrophy, atrophic > muscle, muscular > spinal > hereditary NEC
- Atrophy, atrophic > muscle, muscular > progressive > spinal > adult
- Atrophy, atrophic > muscle, muscular > spinal > scapuloperoneal form
- Atrophy, atrophic > muscle, muscular > spinal > childhood form, type II
- Atrophy, atrophic > muscle, muscular > spinal > juvenile form, type III
Codes in the same group
| Code | Description | Status |
|---|---|---|
| G12.0 | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] | Valid |
| G12.2 | Motor neuron disease | Not billable |
| G12.8 | Other spinal muscular atrophies and related syndromes | Valid |
| G12.9 | Spinal muscular atrophy, unspecified | Valid |