orofacial clefting syndrome rare syndrome with cardiac malformations Thomas syndrome GARD:0005175 ICD10:Q87.8 MESH:C536514 MONDO:0018043 Orphanet:3316 Potter sequence-cleft lip/palate-cardiopathy syndrome SCTID:716740009 Thomas syndrome is characterised by renal anomalies, cardiac malformations and cleft lip or palate. It has been described in six patients. Transmission was suggested to be autosomal recessive. UMLS:C2931225 genetic otorhinolaryngologic disease syndromic renal or urinary tract malformation hereditary connective tissue disorder genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability