Distal Monosomy 9p Syndrome C0265425
Also known as 9p minus syndrome, this involves deletion of genetic material from chromosome 9. It causes distinctive facial features and developmental delays. Care addresses specific symptoms with multidisciplinary support.
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