obsolete_Feingold syndrome true 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) (see these terms). 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. FGLDS orphanet ODED syndrome Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum MMT FS ICD10:Q87.8 Oculo-digito-esophageal-duodenal syndrome Microcephaly - intellectual disability - tracheoesophageal fistula OMIM:614326 OMIM:164280 MODED syndrome Brunner-Winter syndrome 3.41.0 Microcephaly-digital anomalies-normal intelligence syndrome Replaced with Mondo term. Microcephaly - oculo-digito-esophageal-duodenal syndrome http://purl.obolibrary.org/obo/MONDO_0015267