Amelogenesis Imperfecta Type 2a1 C2673922

Published: July 22, 2026Updated: August 20, 2026

A genetic enamel defect causing teeth to appear discolored and have soft enamel. It affects both baby and permanent teeth, managed with restorative dental care.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

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

When to seek medical help

Recognize when you need immediate medical attention.

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Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Medication Comparisons

Compare medications used to treat Amelogenesis Imperfecta Type 2a1 C2673922. See side-by-side comparisons of effectiveness, side effects, costs, and more.

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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 20, 2026. · Read our editorial policy