Ebf3 Related Disorder Cn239924
A genetic condition caused by changes in the EBF3 gene affecting development and nervous system function. It can cause developmental delays, speech issues, and distinctive facial features. Treatment involves developmental therapies and supportive care tailored to individual needs.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Developmental delay
(neurologic)Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Intellectual disability
(neurologic)Hypertonia
(neurologic)Ataxia
(neurologic)Medication Comparisons
Compare medications used to treat Ebf3 Related Disorder Cn239924. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy