G12.0
BillableInfantile spinal muscular atrophy, type I [Werdnig-Hoffman]
Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
Coding Notes
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
- Infantile spinal muscular atrophy64383006
- Progressive muscular atrophy of infancy64383006
- Spinal muscular atrophy type I64383006
- Spinal muscular atrophy, type I64383006
- WHD - Werdnig-Hoffmann disease64383006
- Werdnig-Hoffmann disease64383006
- Anterior horn cell disease85672005
UMLS
- Infantile Muscular AtrophyC5848259
- Infantile Spinal Muscular AtrophyC5848259
- Infantile spinal muscular atrophyC5848259
- Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]C5848259
- MUSCULAR ATROPHY, INFANTILEC5848259
- Muscular Atrophy, InfantileC5848259
- Muscular Atrophy, Spinal, InfantileC5848259
- Muscular Atrophy, Spinal, Type IC5848259
- Progressive muscular atrophy of infancyC5848259
- SMA IC5848259
- SMA, INFANTILE ACUTE FORMC5848259
- SMA, Infantile Acute FormC5848259
- SMA1C5848259
- SPINAL MUSCULAR ATROPHY, TYPE IC5848259
- Severe Infantile Spinal Muscular AtrophyC5848259
- Spinal Muscular Atrophy 1C5848259
- Spinal Muscular Atrophy Type 1C5848259
- Spinal Muscular Atrophy Type IC5848259
- Spinal Muscular Atrophy, InfantileC5848259
- Spinal Muscular Atrophy, Type IC5848259
- Spinal muscular atrophy infantile onsetC5848259
- Spinal muscular atrophy type IC5848259
- Spinal muscular atrophy, type IC5848259
- Type I Spinal Muscular AtrophyC5848259
- WERDNIG HOFFMANN DISC5848259
- WERDNIG-HOFFMANN DISEASEC5848259
- WHD - Werdnig-Hoffmann diseaseC5848259
- Werdnig Hoffman DiseaseC5848259
- Werdnig Hoffmann DiseaseC5848259
- Werdnig Hoffmann diseaseC5848259
- Werdnig-Hoffmann DiseaseC5848259
- Werdnig-Hoffmann diseaseC5848259
- Werdnig-Hoffmann disease (disorder)C5848259
- disease werdnig hoffmansC5848259
- infantile muscular atrophyC5848259
- type i spinal muscular atrophyC5848259
- werdnig hoffman diseaseC5848259
- werdnig hoffmann diseaseC5848259
- werdnig-hoffman diseaseC5848259
- werdnig-hoffmann diseaseC5848259
Frequently Asked Questions
What is the ICD-10 code for infantile spinal muscular atrophy, type i [werdnig-hoffman]?
The ICD-10-CM code for infantile spinal muscular atrophy, type i [werdnig-hoffman] is G12.0. The full clinical description is "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]". G12.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G12.0 mean?
ICD-10-CM code G12.0 represents "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]". 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 G12.0 a billable code?
Yes, G12.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G12.0 in?
G12.0 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G12.0 map to?
G12.0 maps to 3 SNOMED CT concepts: 85672005, 64383006, 5262007. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G12.0?
G12.0 is linked to 1 UMLS Concept Unique Identifier: C5848259. 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.