MeSH Browser

MeSH Supplementary: Oculodigitoesophagoduodenal syndrome
Unique ID: C537734
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537734
Entry Term(s): Brunner Winter syndrome; Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum; Feingold syndrome; MMT Syndrome; MODED syndrome Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome; Microcephaly and Digital Abnormalities with Normal Intelligence; Microcephaly, Mental Retardation, and Tracheoesophageal Fistula Syndrome; Microcephaly-Mesobrachyphalangy-Tracheoesophageal Fistula (MMT) Syndrome; Microcephaly-Oculo-Digito-Esophageal-Duodenal (MODED) Syndrome; Microcephaly-oculo-digito-esophageal-duodenal syndrome; ODED Syndrome; Oculo-Digito-Esophagoduodental (ODED) Syndrome
Registry Number: 0
Heading Mapped to: Eyelids / *abnormalities; *Intellectual Disability; *Microcephaly; *Tracheoesophageal Fistula; *Limb Deformities, Congenital
Frequency: 25
Note: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum; mutation in MYCN
Date of Entry: 2010/08/25
Revision Date: 2019/06/24

Oculodigitoesophagoduodenal syndrome MeSH Supplementary Concept Data 2024