autosomal dominant disease syndromic disease obsolete non-syndromic respiratory or mediastinal malformation Feingold syndrome ODED syndrome UMLS:C0796068 MODED syndrome digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum Feingold syndrome (FS), also known as oculo-digito-esophageal-duodenal (ODED) syndrome, is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies and is comprised of two subtypes: FS type 1 (FS1) and FS type 2 (FS2). FS1 is by far the most common form while FS2 has only been reported in 3 patients and has the same clinical characteristics as FS1, apart from the absence of gastrointestinal atresia and short palpebral fissures. MONDO:0015267 DOID:0060464 GARD:0008407 MMT microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome oculo-digito-esophageal-duodenal syndrome microcephaly-intellectual disability-tracheoesophageal fistula syndrome NCIT:C74987 Brunner-Winter syndrome FGLDS digital anomalies with short palpebral fissures and atresia of esophagus or duodenum OMIMPS:164280 MEDGEN:163209 microcephaly-digital anomalies-normal intelligence syndrome digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum FS Orphanet:1305