has material basis in germline mutation in MYCN Feingold syndrome type 1 https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/feingold_syndrome_1 MODED syndrome type 1 MEDGEN:1637716 Feingold syndrome 1 GARD:0017624 digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum digital anomalies with short palpebral fissures and atresia of esophagus or duodenum SCTID:702431004 ICD9:759.89 Feingold syndrome caused by mutation in MYCN microcephaly-digital anomalies-normal intelligence syndrome type 1 Oded syndrome microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1 microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1 microcephaly-oculo-digito-esophageal-duodenal syndrome MYCN Feingold syndrome Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies. OMIM:164280 oculo-digito-esophageal-duodenal syndrome type 1 Orphanet:391641 ODED syndrome type 1 FGLDS1 microcephaly, intellectual disability, and tracheoesophageal fistula syndrome microcephaly and digital abnormalities with normal intelligence UMLS:C4551774 MONDO:0008115 digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1 microcephaly, mental retardation, and tracheoesophageal fistula syndrome Mmt syndrome FS1 oculodigitoesophagoduodenal syndrome MMT type 1 Brunner-Winter syndrome type 1 Feingold syndrome digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1 Feingold syndrome type 1 Feingold syndrome