Oculo-digito-oesophageal-duodenal syndrome

Preferred Label : Oculo-digito-oesophageal-duodenal syndrome;

ICD-11 definition : Oculo-digito-esophageal-duodenal syndrome (ODED) is a multiple congenitalanomalies syndrome characterised by the association of variable degrees of microcephaly with or without learning disabilities, short palpebral fissures, a deep nasal bridge with anteverted nostrils, ear anomalies and micrognathia, anomalies of the hands and feet, and oesophageal/duodenal atresia.;

ICD-11 synonym : ODOD - [Oculo-digito-oesophageal-duodenal syndrome];

ICD-11 acronym : ODOD;

Détails

Origin ID

1180436726;

Automatic exact mappings (from CISMeF team)
- Oculodentodigital dysplasia [OMIM Phenotype]
- gap junction protein alpha 1 [ORDO Gene]
Currated CISMeF NLP mapping
- Feingold Syndrome [NCIt concept]
- Feingold syndrome [ORDO Disease]
- Feingold syndrome [MedDRA LLT]
- Feingold syndrome [DO Concept]
- Feingold syndrome [OMIM phenotypic series]
- 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 [MeSH concept]
- oculodigitoesophagoduodenal syndrome [MeSH Supplementary Concept]
- oculodigitoesophagoduodenal syndrome [Disease (Nov.)]

Position du mot-clé dans l'(les) arborescence(s) :

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