- Autosomal recessive hereditary disorder
- Cerebellar ataxia
- Hereditary ataxia
- Hereditary disorder of nervous system
- Hereditary disorder of the visual system
- Oculomotor apraxia
Name: Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
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- Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder)
- AOA2 - ataxia oculomotor apraxia type 2
- SCAR1 - spinocerebellar ataxia autosomal recessive 1
- Spinocerebellar ataxia with axonal neuropathy type 2
- Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
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Concept ID: 725408001- AOA2 - ataxia oculomotor apraxia type 2
- SCAR1 - spinocerebellar ataxia autosomal recessive 1
- Spinocerebellar ataxia with axonal neuropathy type 2
- Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
Hide descriptions.
Read Codes:
ICD-10 Codes: H518 G602