G12.1 is the ICD-10 code for Other inherited spinal muscular atrophy. It is a four-character subcategory of G12 (Spinal muscular atrophy and related syndromes), the most specific level in the WHO edition. It belongs to the block G10–G14 (Systemic atrophies primarily affecting the central nervous system) in Chapter VI, Diseases of the nervous system.
- Code type
- Subcategory (4 characters)
- Chapter
- VI · G00–G99
- Classification
- WHO ICD-10, 2019 version
What G12.1 includes
Conditions and terms that are coded here.
- Progressive bulbar palsy of childhood [Fazio-Londe]
- Spinal muscular atrophy:
- adult form
- childhood form, type II
- distal
- juvenile form, type III [Kugelberg-Welander]
- scapuloperoneal form
G12.1 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
G12.1Annan hereditär spinal muskelatrofi
- G12.1AHereditär spinal muskelatrofi, seninfantil typ II
- G12.1BHereditär spinal muskelatrofi, juvenil typ III
- G12.1WAnnan hereditär spinal muskelatrofi
G12.1Annen arvelig spinal muskelatrofi
DG121Anden arvelig spinal muskelatrofi
- DG121AAtrophia musculorum spinalis, voksen form
- DG121BAtrophia musculorum spinalis, skapuloperoneal form
- DG121CAtrophia musculorum spinalis, distal form
- DG121DAtrophia musculorum spinalis, type II
- DG121EAtrophia musculorum spinalis, type III
- DG121FProgressiv bulbær parese hos barn
G12.1Muu perinnöllinen spinaalinen lihasatrofia
G12.1Sonstige vererbte spinale Muskelatrophie
G12.1Autres amyotrophies spinales héréditaires
G12.1overige erfelijke-vormen van spinale spieratrofie
G12.1Other inherited spinal muscular atrophy
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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