702431004: Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Feingold syndrome

Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2995031014	Feingold syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2995045015	Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2995323014	Microcephaly-oculo-digito-esophageal-duodenal syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2995393016	Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3009702015	Microcephaly-oculo-digito-oesophageal-duodenal syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3009804010	Oculo-digito-oesophagoduodenal syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3009846018	Oculo-digito-esophagoduodenal syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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