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van der woude syndrome

Medical Definition

A rare autosomal dominant syndrome caused by mutations in the irf6 gene. it is characterized by a cleft palate and/or pits on the lower lip. other signs and symptoms include absent teeth, palate and tongue deformities.
Related Codes (1)
Code
Description
Billable
Details
Q38.0Congenital malformations of lips, not elsewhere classified
Type 1 Excludes (4)

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