Monosomy 13q34 C4707797
A chromosomal condition where a portion of chromosome 13 is missing. It can cause developmental delays, distinctive facial features, and other health concerns. Care focuses on supportive management.
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 20, 2026. · Read our editorial policy