Q36.9
ICD-10-CMThis code describes a congenital malformation characterized by a split or opening in the upper lip on one side, resulting from incomplete fusion during fetal development. It can range in severity from a small notch to a complete separation extending into the nostril. This condition often affects feeding, speech, and facial aesthetics.
Use this code for documented cases of a cleft lip that is specifically identified as unilateral, without further specification of its completeness or the presence of a cleft palate. Documentation should clearly state "unilateral cleft lip" or similar terminology. This code is appropriate when the laterality is known but the extent (e.g., incomplete, complete) is not specified.
AI-generated reference. Verify against official guidelines.
Clinical Notes
Inclusion Terms
Code History
Change History