Alphabetic Index · main term
Werdnig-Hoffmann syndrome (muscular atrophy)
Werdnig-Hoffmann syndrome (muscular atrophy) is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists G12.0 for this term: Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
Other Index terms that lead to G12.0
Different words, same code. 8 entries
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), infantile spinal
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), progressive (bulbar), infantile (spinal)
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), progressive (bulbar), spinal, infantile
- Atrophy, atrophic (of), muscle, muscular (diffuse) (general) (idiopathic) (primary), spinal, infantile, type I (Werdnig-Hoffmann)
- Atrophy, atrophic (of), Werdnig-Hoffmann
- Disease, diseased, Werdnig-Hoffmann
- Syndrome, Hoffmann-Werdnig
- Syndrome, Werdnig-Hoffman