G12.1
BillableOther inherited spinal muscular atrophy
Other inherited spinal muscular atrophy
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
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- Progressive spinal muscular atrophy5262007
- SMA - Spinal muscular atrophy5262007
- Spinal muscular atrophy5262007
- Dandy-Walker deformity14447001
- Dandy-Walker malformation14447001
- Dandy-Walker syndrome14447001
- Chronic respiratory failure39871006
- Familial spinal muscular atrophy54280009
- Juvenile spinal muscular atrophy54280009
- Kugelberg-Welander disease54280009
- SMA type III54280009
- SMA354280009
- Spinal muscular atrophy type III54280009
- Spinal muscular atrophy, type III54280009
- Bulbar palsy54304004
- Bulbar paralysis54304004
- PBP - Progressive bulbar palsy54304004
- Progressive bulbar palsy54304004
- Adult onset spinal muscular atrophy85505000
- Adult spinal muscular atrophy85505000
- Generalised spinal muscular atrophy of late onset85505000
- Generalized spinal muscular atrophy of late onset85505000
- Duchenne-Aran muscular atrophy88923002
- PMA - Progressive muscular atrophy88923002
- Progressive muscular atrophy88923002
- Pure progressive muscular atrophy88923002
- Upper motor neuron disease95647008
- Late infantile spinal muscular atrophy128212001
- SMA2128212001
- Spinal muscular atrophy type II128212001
- Spinal muscular atrophy, type II128212001
- Fazio-Londe syndrome230246005
- Progressive bulbar palsy of childhood230246005
- Distal spinal muscular atrophy230247001
- Scapuloperoneal spinal muscular atrophy230248006
- Scapulohumeral spinal muscular atrophy230251004
- Congenital anterior polar cataract253224008
- Autosomal recessive distal spinal muscular atrophy 1711483003
- Diaphragmatic spinal muscular atrophy711483003
- Distal hereditary motor neuronopathy type VI711483003
- Distal spinal muscular atrophy type 1711483003
- Severe infantile axonal neuropathy with respiratory failure711483003
- Spinal muscular atrophy with respiratory distress711483003
- Spinal muscular atrophy with respiratory distress type 1711483003
- Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome723612001
- Autosomal dominant benign distal spinal muscular atrophy763067000
- Autosomal dominant congenital benign spinal muscular atrophy763067000
- Congenital benign spinal muscular atrophy with contracture763067000
- Congenital nonprogressive spinal muscular atrophy763067000
- Autosomal recessive distal spinal muscular atrophy type 2763533003
- Distal hereditary motor neuropathy Jerash type763533003
- ATP7A (ATPase copper transporting alpha) related distal motor neuropathy766764008
- X-linked distal hereditary motor neuropathy type 3766764008
- X-linked distal spinal muscular atrophy type 3766764008
- Autosomal recessive distal spinal muscular atrophy type 3770430000
- Distal spinal muscular atrophy type 3770430000
- Diaphragmatic spinal muscular atrophy type 2770727008
- SMARD2 - spinal muscular atrophy with respiratory distress type 2770727008
- Severe infantile axonal neuropathy with respiratory failure type 2770727008
- Spinal muscular atrophy with respiratory distress type 2770727008
- X-linked spinal muscular atrophy with respiratory distress770727008
- Hamano Tsukamoto syndrome771238004
- Spinal atrophy, ophthalmoplegia, pyramidal syndrome771238004
- Autosomal dominant childhood-onset proximal spinal muscular atrophy772129007
- Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy772129007
- SMALED - spinal muscular atrophy, lower extremity, dominant772129007
- Spinal muscular atrophy with lower extremity predominance772129007
- Autosomal dominant adult-onset proximal spinal muscular atrophy784391002
- Autosomal dominant late-onset spinal muscular atrophy Finkel type784391002
- Finkel disease784391002
- SMAFK - spinal muscular atrophy Finkel type784391002
- Autosomal dominant distal hereditary motor neuropathy1156837002
- X-linked distal hereditary motor neuropathy1156840002
- Autosomal recessive distal hereditary motor neuropathy1156850001
- Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome1172588008
UMLS
- AMYOTROPHY, NEUROGENIC SCAPULOPERONEAL, NEW ENGLAND TYPEC0751335
- Amyotrophy, Neurogenic Scapuloperoneal, New England TypeC0751335
- SCAPULOPERONEAL SPINAL MUSCULAR ATROPHYC0751335
- SPINAL MUSCULAR ATROPHY, SCAPULOPERONEALC0751335
- SPSMAC0751335
- Scapuloperoneal Form of Spinal Muscular AtrophyC0751335
- Scapuloperoneal Spinal Muscular AtrophyC0751335
- Scapuloperoneal form spinal muscular atrophyC0751335
- Scapuloperoneal spinal muscular atrophyC0751335
- Scapuloperoneal spinal muscular atrophy (disorder)C0751335
- Spinal Muscular Atrophy, ScapuloperonealC0751335
- Spinal Muscular Atrophy, Scapuloperoneal FormC0751335
- Adult form spinal muscular atrophyC1838230
- SMA4C1838230
- SPINAL MUSCULAR ATROPHY, ADULT FORMC1838230
- SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL RECESSIVEC1838230
- SPINAL MUSCULAR ATROPHY, TYPE IVC1838230
- Spinal Muscular Atrophy, Adult FormC1838230
- Spinal Muscular Atrophy, Proximal, Adult, Autosomal RecessiveC1838230
- Spinal Muscular Atrophy, Type IVC1838230
- Spinal muscular atrophy type IVC1838230
- BULBAR PALSY, PROGRESSIVE, OF CHILDHOODC0393540
- Bulbar Palsy, Progressive, Of ChildhoodC0393540
- Childhood Progressive Bulbar PalsyC0393540
- Disease, Fazio-LondeC0393540
- Disease, Fazio-Londe'sC0393540
- FAZIO-LONDE DISEASEC0393540
- Fazio Londe DiseaseC0393540
- Fazio Londe SyndromeC0393540
- Fazio Londe's DiseaseC0393540
- Fazio Londe's SyndromeC0393540
- Fazio-Londe DiseaseC0393540
- Fazio-Londe SyndromeC0393540
- Fazio-Londe diseaseC0393540
- Fazio-Londe syndromeC0393540
- Fazio-Londe's DiseaseC0393540
- Fazio-Londe's SyndromeC0393540
- Progressive Bulbar Palsy of ChildhoodC0393540
- Progressive bulbar palsy of childhoodC0393540
- Progressive bulbar palsy of childhood (disorder)C0393540
- Progressive bulbar palsy of childhood [Fazio-Londe]C0393540
- Syndrome, Fazio-LondeC0393540
- Syndrome, Fazio-Londe'sC0393540
- Childhood form, type II spinal muscular atrophyC2875050
- Distal Spinal Muscular AtrophyC0393541
- Distal spinal muscular atrophyC0393541
- Distal spinal muscular atrophy (disorder)C0393541
- Spinal Muscular Atrophy, DistalC0393541
- Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]C2875051
- Other Inherited Spinal Muscular AtrophyC0477349
- Other inherited spinal muscular atrophyC0477349
Frequently Asked Questions
What is ICD-10 code G12.1?
ICD-10-CM code G12.1 represents "Other inherited spinal muscular atrophy". It 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.
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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.