Q10-Q18: Congenital malformations of eye, ear, face and neck
Q18: Other congenital malformations of face and neck
The condition group titled "Other congenital malformations of face and neck" includes various disorders that are present at birth and affect the development of the face or neck. These malformations can result from genetic factors, environmental influences during pregnancy, or a combination of both. The specific malformations, symptoms, and impacts on health can vary widely among individuals depending on the particular condition within this group. Some might alter the physical appearance of the face or neck without impacting bodily functions, while others might cause difficulties with eating, breathing, hearing, or speech. The progression of these conditions often depends on the nature and severity of the abnormalities, which can range from mild and practically invisible to severe and potentially life-altering. It's important to remember that early detection and proactive care can help manage many of these conditions.
Subcodes of Q18:
- Q18.0: Sinus, fistula and cyst of branchial cleft
- Q18.1: Preauricular sinus and cyst
- Q18.2: Other branchial cleft malformations
- Q18.3: Webbing of neck
- Q18.4: Macrostomia
- Q18.5: Microstomia
- Q18.6: Macrocheilia
- Q18.7: Microcheilia
- Q18.8: Other specified congenital malformations of face and neck
- Q18.9: Congenital malformation of face and neck, unspecified
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If you see an ICD diagnosis code (e.g., on a medical report), be aware that doctors may also include additional indicators to express diagnostic certainty. Only a healthcare professional can interpret these codes accurately in the context of your individual case.
For a complete understanding of your condition and what the diagnosis means for you, please speak directly with your doctor.