Rosselli-Gulienetti syndrome
MONDO:0009148Mondo
Findings
No curated finding names Rosselli-Gulienetti syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A rare congenital ectodermal dysplasia syndrome with a range of signs and symptoms including cleft lip or palate, mental retardation and various forms of ectodermal dysplasia. Additional symptoms may include fused eyelids, absent nails, delayed bone growth and dry skin. It is believed that this syndrome follows an autosomal dominant pattern of inheritance with incomplete penetrance, and caused by a mutation affecting the TP63 gene
Definition from the Mondo Disease Ontology (MONDO:0009148), read 2026-09-29. CC BY 4.0.