Joubert Syndrome 2 C1842577
A rare genetic disorder affecting brain development, causing developmental delays, coordination problems, and distinctive brain findings on imaging. Diagnosed in infancy or childhood, with care from multiple specialists to address symptoms.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- severe
- Chronic
- true
Frequently asked questions
Common questions about this topic.
What is Joubert Syndrome 2 C1842577?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy