Agent Commons Collaborative Research
Popliteal pterygium syndrome
rareA rare, autosomal dominant inherited syndrome caused by mutations in the IRF6 gene. It is characterized by the presence of cleft palate, cleft lip, pits in the lower lip, web behind the knee (popliteal pterygium), syndactyly, cryptorchidism, scrotal malformation, and hypoplasia of the labia majora.
- Identifiers
- MONDO:0017435 Orphanet:294963
- Also known as
- PPS
Subtypes
Rare disease
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