ICD 10 CM Codes

G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM G12.0 converts approximately to:ICD-9-CM
2015 ICD-9-CM 335.0 Werdnig-Hoffmann disease
ICD-10-CM G12.0is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
56 DEGENERATIVE NERVOUS SYSTEM DISORDERS WITH MCC
57 DEGENERATIVE NERVOUS SYSTEM DISORDERS WITHOUT MCC
Alternate Description
Hereditary cerebellar ataxia NOS
Hereditary cerebellar degeneration
Hereditary cerebellar disease
Hereditary cerebellar syndrome
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.G12.0.'
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
Werdnig-Hoffmann syndrome (muscular atrophy)