oculodigitoesophagoduodenal syndrome

Preferred Label : oculodigitoesophagoduodenal syndrome;

MeSH note : Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum; mutation in MYCN;

MeSH synonym : feingold syndrome; microcephaly-oculo-digito-esophageal-duodenal syndrome; brunner winter syndrome; digital anomalies with short palpebral fissures and atresia of esophagus or duodenum; microcephaly and digital abnormalities with normal intelligence; MMT syndrome; ODED syndrome; microcephaly, mental retardation, and tracheoesophageal fistula syndrome; Oculo-Digito-Esophagoduodental (ODED) syndrome; Microcephaly-Mesobrachyphalangy-Tracheoesophageal fistula (MMT) syndrome; Microcephaly-Oculo-Digito-Esophageal-Duodenal (MODED) syndrome; MODED syndrome Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome;

Details

Origin ID

C537734;

UMLS CUI

C0796068;

Currated CISMeF NLP mapping
- Feingold Syndrome [NCIt concept]
- Feingold syndrome [DO Concept]
- Feingold syndrome [OMIM phenotypic series]
- Feingold syndrome [MedDRA LLT]
- Feingold syndrome [ORDO Disease]
- Feingold syndrome 1 [OMIM Phenotype]
- Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder) [SNOMED CT concept]
- Oculo-digito-esophageal-duodenal syndrome [MedDRA LLT]
- Oculo-digito-oesophageal-duodenal syndrome [MedDRA Preferred Term]
- Oculo-digito-oesophageal-duodenal syndrome [ICD-11 More detail]
- oculodigitoesophagoduodenal syndrome [Disease (Nov.)]
DO Cross reference
- Feingold syndrome [DO Concept]
MeSH term(s) associated for indexing
- eyelids [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- limb deformities, congenital [MeSH Descriptor]
- microcephaly [MeSH Descriptor]
- tracheoesophageal fistula [MeSH Descriptor]
Record concept(s)
- Oculodigitoesophagoduodenal syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Feingold Syndrome [NCIt concept]
- Feingold syndrome [ORDO Disease]
- Feingold syndrome [DO Concept]
- Feingold syndrome [MedDRA LLT]
- Feingold syndrome 1 [OMIM Phenotype]
- Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder) [SNOMED CT concept]
- Oculo-digito-esophageal-duodenal syndrome [MedDRA LLT]
- Oculo-digito-oesophageal-duodenal syndrome [MedDRA Preferred Term]
- oculodigitoesophagoduodenal syndrome [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

Main resources

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