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ICD-10 diagnosis code

G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

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G12.0 is the ICD-10 code for Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]. 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

G12.0 in national editions

Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.

SwedenICD-10-SE

G12.0Infantil spinal muskelatrofi, typ I [Werdnig-Hoffman]

NorwayICD-10-NO

G12.0Infantil spinal muskelatrofi, type I

DenmarkICD-10-DK

DG120Atrophia musculorum spinalis, type I

FinlandICD-10-FI

G12.0Lapsuuden spinaalinen lihasatrofia, tyyppi I (Werdnig-Hoffmann)

GermanyICD-10-GM

G12.0Infantile spinale Muskelatrophie, Typ I [Typ Werdnig-Hoffmann]

FranceICD-10-FR

G12.0Amyotrophie spinale infantile, type I [Werdnig–Hoffman]

NetherlandsICD-10-NL

G12.0infantiele spinale-spieratrofie, type I [Werdnig-Hoffman]

United StatesICD-10-CM

G12.0Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

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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