Pontocerebellar Hypoplasia Type 7 C3554226
A genetic condition causing incomplete brain development before birth. It leads to severe intellectual disability and movement disorders. Treatment involves supportive care addressing the various symptoms.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- severe
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 26, 2026. · Read our editorial policy