Alphabetic Index · main term
Fazio-Londe disease or syndrome
Fazio-Londe disease or syndrome is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists G12.1 for this term: Other inherited spinal muscular atrophy. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Other inherited spinal muscular atrophy
Other Index terms that lead to G12.1
Different words, same code. 10 entries
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), progressive (bulbar), adult
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), progressive (bulbar), spinal, adult
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), spinal, adult form
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), spinal, childhood form, type II
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), spinal, distal
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), spinal, hereditary NEC
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), spinal, juvenile form, type III (Kugelberg- Welander)
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), spinal, scapuloperoneal form
- Kugelberg-Welander disease
- Palsy, bulbar (progressive) (chronic), of childhood (Fazio-Londe)