Cleft lip (Q36)
The ICD-10 code Q36 identifies different types of cleft lip, a congenital condition where there is a split in the upper lip. This section covers various forms of cleft lip, including bilateral (Q36.0), median (Q36.1), and unilateral (Q36.9) presentations.
The ICD-10 code for cleft lip helps medical coders and healthcare professionals accurately classify specific lip clefts, aiding in diagnosis and treatment planning. The bilateral cleft lip (Q36.0) refers to clefts affecting both sides of the lip and can be complete or incomplete, sometimes involving the alveolar process of the maxilla. The term “bilateral cleft lip” or descriptive phrases like “complete left cleft lip and incomplete right cleft lip” are all captured under this code. The median cleft lip (Q36.1) describes a rare midline deformity, also known as “central cleft lip” or associated with conditions like Pai syndrome and frontonasal dysplasia. Meanwhile, the unilateral cleft lip (Q36.9) involves a cleft on one side, with synonyms including “right cleft lip,” “left cleft lip,” or “cleft lip and cleft of alveolar process,” covering both complete and incomplete variations. Using these codes correctly ensures clear communication about the specific type of cleft lip being treated or studied.
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Cleft lip and cleft palate (Q35-Q37)
Q36 Cleft lip
- Q36.0 Cleft lip, bilateral
- Q36.1 Cleft lip, median
- Q36.9 Cleft lip, unilateral
Cleft lip (Q36)
Instructional Notations
Includes
This note appears immediately under a three character code title to further define, or give examples of, the content of the category.
- cheiloschisis
- congenital fissure of lip
- harelip
- labium leporinum
Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- cleft lip with cleft palate Q37
Clinical Terms
The following clinical terms provide additional context, helping users better understand the clinical background and common associations for each diagnosis listed in this section. Including related terms alongside ICD-10-CM codes supports coders, billers, and healthcare professionals in improving accuracy, enhancing documentation, and facilitating research or patient education.
Cleft Lip
Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region.