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Distal 10q Deletion Syndrome C2674937

Published: July 22, 2026Updated: August 25, 2026

A chromosomal disorder where a piece of chromosome 10 is missing, affecting development and causing various health issues. Features may include developmental delay, distinctive facial features, and organ abnormalities. Early intervention and supportive therapies help manage symptoms.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

Key facts at a glance

ICD-10
Q89.9
ICD-11
LA00.0
Body system
congenital
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Congenital heart defect

(cardiovascular)

Generalized symptoms

(congenital)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Intellectual disability

(neurological)

Renal anomalies

(renal)

Microcephaly

(craniofacial)

Medication Comparisons

Compare medications used to treat Distal 10q Deletion Syndrome C2674937. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy