Auriculocondylar Syndrome 2b C5830664
A rare genetic condition affecting craniofacial development, causing abnormalities in the jaw and ears. Treatment typically involves surgical correction and multidisciplinary care.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy