- Autosomal recessive hereditary disorder
- Cerebellar ataxia
- Dysgenesis of the cerebellum (disorder)
- Hereditary ataxia
- Hereditary disorder of nervous system
- Hereditary disorder of the visual system
- Intellectual disability
- Multiple system malformation syndrome (disorder)
- Oculomotor apraxia
Name: Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)
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- Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
- Poretti Boltshauser syndrome
- Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)
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Concept ID: 763344007- Poretti Boltshauser syndrome
- Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)
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Read Codes:
ICD-10 Codes: G111