G12.1

Billable

Other inherited spinal muscular atrophy

Other inherited spinal muscular atrophy

Status

Billable / Specific

Block

G10-G14

Parent Code

G12

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • 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

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(4)
G12.0

Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

BillableG12.2

Motor neuron disease

G12.8

Other spinal muscular atrophies and related syndromes

BillableG12.9

Spinal muscular atrophy, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

8B61.ZSpinal muscular atrophy, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(233)

SNOMED CT

UMLS

Clinical Terms

  • SMA2
  • X-linked distal spinal muscular atrophy type 3
  • ATP7A (ATPase copper transporting alpha) related distal motor neuropathy
  • PMA - Progressive muscular atrophy
  • Autosomal dominant adult-onset proximal spinal muscular atrophy
  • SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL
  • Fazio Londe Syndrome
  • Fazio-Londe syndrome
  • Bulbar palsy
  • Fazio-Londe's Syndrome
  • Diaphragmatic spinal muscular atrophy type 2
  • Distal spinal muscular atrophy
  • Kugelberg-Welander disease
  • FAZIO-LONDE DISEASE
  • Spinal Muscular Atrophy, Scapuloperoneal Form
  • Spinal Muscular Atrophy, Proximal, Adult, Autosomal Recessive
  • Progressive muscular atrophy
  • Autosomal dominant congenital benign spinal muscular atrophy
  • Disease, Fazio-Londe's
  • Scapuloperoneal form spinal muscular atrophy
  • Severe infantile axonal neuropathy with respiratory failure type 2
  • Fazio Londe's Disease
  • Amyotrophy, Neurogenic Scapuloperoneal, New England Type
  • Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
  • Congenital benign spinal muscular atrophy with contracture
  • Pure progressive muscular atrophy
  • Fazio Londe Disease
  • SMA - Spinal muscular atrophy
  • Autosomal recessive distal spinal muscular atrophy type 2
  • Distal hereditary motor neuronopathy type VI
  • Fazio-Londe's Disease
  • Bulbar paralysis
  • Fazio Londe's Syndrome
  • SPINAL MUSCULAR ATROPHY, TYPE IV
  • X-linked spinal muscular atrophy with respiratory distress
  • Late infantile spinal muscular atrophy
  • Spinal muscular atrophy, type II
  • Spinal muscular atrophy, type III
  • Autosomal dominant distal hereditary motor neuropathy
  • Spinal atrophy, ophthalmoplegia, pyramidal syndrome
  • X-linked distal hereditary motor neuropathy type 3
  • PBP - Progressive bulbar palsy
  • Autosomal recessive distal spinal muscular atrophy 1
  • Spinal muscular atrophy with respiratory distress
  • BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD
  • Upper motor neuron disease
  • Progressive Bulbar Palsy of Childhood
  • Progressive bulbar palsy of childhood (disorder)
  • Spinal muscular atrophy with respiratory distress type 2
  • Spinal muscular atrophy
  • Scapuloperoneal Spinal Muscular Atrophy
  • SMA3
  • Diaphragmatic spinal muscular atrophy
  • Syndrome, Fazio-Londe
  • Hamano Tsukamoto syndrome
  • Childhood form, type II spinal muscular atrophy
  • Duchenne-Aran muscular atrophy
  • Autosomal dominant benign distal spinal muscular atrophy
  • Spinal Muscular Atrophy, Distal
  • Dandy-Walker malformation
  • Childhood Progressive Bulbar Palsy
  • Congenital nonprogressive spinal muscular atrophy
  • Spinal muscular atrophy type III
  • Scapulohumeral spinal muscular atrophy
  • Dandy-Walker deformity
  • SPSMA
  • Progressive bulbar palsy of childhood [Fazio-Londe]
  • Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]
  • Adult form spinal muscular atrophy
  • Congenital anterior polar cataract
  • Distal hereditary motor neuropathy Jerash type
  • Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome
  • Autosomal dominant late-onset spinal muscular atrophy Finkel type
  • Severe infantile axonal neuropathy with respiratory failure
  • Syndrome, Fazio-Londe's
  • Juvenile spinal muscular atrophy
  • Generalised spinal muscular atrophy of late onset
  • Progressive bulbar palsy
  • SMA4
  • Adult onset spinal muscular atrophy
  • Generalized spinal muscular atrophy of late onset
  • Progressive spinal muscular atrophy
  • Distal spinal muscular atrophy type 3
  • Adult spinal muscular atrophy
  • SMARD2 - spinal muscular atrophy with respiratory distress type 2
  • Autosomal recessive distal spinal muscular atrophy type 3
  • Autosomal recessive distal hereditary motor neuropathy
  • Familial spinal muscular atrophy
  • Spinal muscular atrophy with lower extremity predominance
  • Disease, Fazio-Londe
  • Autosomal dominant childhood-onset proximal spinal muscular atrophy
  • Spinal muscular atrophy type II
  • X-linked distal hereditary motor neuropathy
  • Distal spinal muscular atrophy type 1
  • SMALED - spinal muscular atrophy, lower extremity, dominant
  • Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy
  • Dandy-Walker syndrome
  • Spinal Muscular Atrophy, Adult Form
  • Spinal muscular atrophy type IV
  • Scapuloperoneal spinal muscular atrophy (disorder)
  • Spinal muscular atrophy with respiratory distress type 1
  • Chronic respiratory failure
  • Finkel disease
  • SMAFK - spinal muscular atrophy Finkel type
  • Scapuloperoneal Form of Spinal Muscular Atrophy
  • Distal spinal muscular atrophy (disorder)
  • SMA type III
Frequently Asked Questions
What is the ICD-10 code for other inherited spinal muscular atrophy?

The ICD-10-CM code for other inherited spinal muscular atrophy is G12.1. The full clinical description is "Other inherited spinal muscular atrophy". G12.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G12.1 mean?

ICD-10-CM code G12.1 represents “Other inherited spinal muscular atrophy”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.

Is G12.1 a billable code?

Yes, G12.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G12.1 in?

G12.1 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What SNOMED CT codes does G12.1 map to?

G12.1 maps to 28 SNOMED CT concepts: 766764008, 85505000, 784391002, 763067000, 772129007, and 23 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G12.1?

G12.1 is linked to 7 UMLS Concept Unique Identifiers: C0751335, C1838230, C0393540, C2875050, C0393541, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G12.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other inherited spinal muscular atrophy affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of G12.1?

G12.1 maps to the ICD-11 code: 8B61.Z (Spinal muscular atrophy, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.