ICD-10 diagnosis code

G11.0 Congenital nonprogressive ataxia

This page in Swedish

G11.0 is the ICD-10 code for Congenital nonprogressive ataxia. It is a four-character subcategory of G11 (Hereditary ataxia), 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

G11.0 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

G11.0Medfödd icke progressiv ataxi

NorwayICD-10-NO

G11.0Medfødt ikke-progressiv ataksi

DenmarkICD-10-DK

DG110Ataxia nonprogressiva congenita

FinlandICD-10-FI

G11.0Synnynnäinen ei-etenevä ataksia

  • G11.00Pikkuaivojen dysplasia and aplasia
  • G11.01Joubert oireyhtymä
  • G11.02Epätasapaino-oireyhtymä
  • G11.08Muu synnynnäinen ei-etenevä ataksia
GermanyICD-10-GM

G11.0Angeborene nichtprogressive Ataxie

FranceICD-10-FR

G11.0Ataxie congénitale non progressive

NetherlandsICD-10-NL

G11.0congenitale ataxie, niet progressief

United StatesICD-10-CM

G11.0Congenital nonprogressive ataxia

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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