World Of Taxonomy
C157576Level 6

Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant condition caused by mutation(s) in the TP63 gene, encoding tumor protein 63. It is characterized by congenital ectodermal dysplasia, ankyloblepharon filiforme adnatum, and cleft lip/palate.

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