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ICD-10-CM Codes G00-G99 G10-G14 G12 G12.1

ICD-10-CM Diagnosis Code G12.1

Effective Date: 10/01/2015 To 09/30/2025

Other inherited spinal muscular atrophy

CMS-HCC-V24	CMS-HCC-V28	RxHCC	Age	Gender	Maternity	Acute or Chronic	MCC
72	190	155	--	--	--	Chronic	No

Applicable To for G12.1:

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

Back-references to G12.1

Atrophy, atrophic(of)

muscle, muscular(diffuse) (general) (idiopathic) (primary) M62.50
- progressive(bulbar) G12.21
  - adult G12.1
  - spinal G12.25
    - adult G12.1
- spinal G12.9
  - adult form G12.1
  - childhood form, type II G12.1
  - distal G12.1
  - hereditary NEC G12.1
  - juvenile form, type III(Kugelberg- Welander) G12.1
  - scapuloperoneal form G12.1

Fazio-Londe disease or syndrome G12.1

Kugelberg-Welander disease G12.1

Palsy see also Paralysis G83.9

bulbar(progressive) (chronic) G12.22
- of childhood(Fazio-Londe) G12.1

Related Medications for G12.1

nusinersen

Chapter, Section and Diagnosis Prefix for G12.1

Diseases of the nervous system

Systemic atrophies primarily affecting the central nervous system

Spinal muscular atrophy and related syndromes