Overview
Congenital cerebellar hypoplasia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
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Lissencephaly co-occurrent with congenital cerebellar hypoplasia(child)
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration(child)
X-linked intellectual disability with cerebellar hypoplasia syndrome(child)
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Zaki Gleeson syndrome(child)
Isolated cerebellar vermis hypoplasia(child)
X-linked intellectual disability Kroes type(child)
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Congenital muscular dystrophy with cerebellar involvement(child)
Curatolo Cilio Pessagno syndrome(child)
Endosteal hyperostoses with cerebellar hypoplasia(child)
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation(child)
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome(child)
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome(child)
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Quick Facts
- SNOMED CT
- 16026008
- UMLS CUI
- C0266470
- Fully Specified Name
- Congenital cerebellar hypoplasia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.