Lambert syndrome https://rarediseases.info.nih.gov/diseases/3169/lambert-syndrome https://www.malacards.org/card/lambert_syndrome Lambert syndrome is a very rare syndrome described in four sibs of one French family and characterized by branchial dysplasia (malar hypoplasia, macrostomia, preauricular tags and meatal atresia), club feet, inguinal herniae and cholestasis due to paucity of interlobular bile ducts and intellectual deficit. SCTID:732961003 branchial dysplasia clubfoot inguinal hernia and biliary atresia MEDGEN:343381 OMIM:245550 branchial dysplasia-intellectual disability-inguinal hernia syndrome UMLS:C1855551 GARD:0003169 MESH:C538396 Orphanet:1296 branchial dysplasia, clubfoot, inguinal hernia, and biliary atresia MONDO:0009507 Lambert syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability