Feingold syndrome type 1
Also known as: Brunner-Winter syndrome type 1, FGLDS1, FS1, Feingold syndrome, Feingold syndrome 1, Feingold syndrome caused by mutation in MYCN, Feingold syndrome type 1, MMT type 1, MODED syndrome type 1, MYCN Feingold syndrome, Mmt syndrome, ODED syndrome type 1, Oded syndrome, digital anomalies with short palpebral fissures and atresia of esophagus or duodenum, digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1, digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum, digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1, microcephaly and digital abnormalities with normal intelligence, microcephaly, intellectual disability, and tracheoesophageal fistula syndrome, microcephaly, mental retardation, and tracheoesophageal fistula syndrome, microcephaly-digital anomalies-normal intelligence syndrome type 1, microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1, microcephaly-oculo-digito-esophageal-duodenal syndrome, microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1, oculo-digito-esophageal-duodenal syndrome type 1, oculodigitoesophagoduodenal syndrome