Distal 17p13 1 Microdeletion Syndrome C4749349
A rare chromosomal disorder involving deletion of genetic material from chromosome 17, impacting development and health. Symptoms can include developmental delay, distinctive facial features, and neurological issues. Treatment focuses on managing specific symptoms with supportive care.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- severe
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy