ICD 10 CM Codes

G12.1 Other inherited spinal muscular atrophy
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM G12.1 converts approximately to:ICD-9-CM
2015 ICD-9-CM 335.11 Kugelberg-Welander disease
ICD-10-CM G12.1is 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
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
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.G12.1.'
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
Fazio-Londe disease or syndrome
Kugelberg-Welander disease
Palsy; bulbar (progressive) (chronic); of childhood (Fazio-Londe)