Hereditary ataxia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A group of genetic disorders characterised by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements
exclusions
sections/codes in this section (8A03.1-8A03.1)
- Friedreich ataxia (8A03.10)
- Ataxia due to Cerebrotendinous xanthomatosis (8A03.11)
- Ataxia due to Refsum disease (8A03.12)
- Ataxia due to abetalipoproteinemia (8A03.13)
- Hereditary episodic ataxia (8A03.14)
- Ataxia due to mitochondrial mutations (8A03.15)
- Spinocerebellar ataxia (8A03.16)
- Other specified hereditary ataxia (8A03.1Y)
- Hereditary ataxia, unspecified (8A03.1Z)
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