ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Rosselli-Gulienetti syndrome https://github.com/monarch-initiative/mondo/issues/432 https://www.malacards.org/card/rosselli_gulienetti_syndrome MEDGEN:163221 MONDO:0009148 Orphanet:90339 Rosselli-Gulienetti syndrome 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 GARD:0024650 UMLS:C0796139 MESH:C563117 icd11.foundation:1430451924 OMIM:225000