699754008: Oculodental syndrome (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2985622010	Oculodental syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
2985765019	Rutherfurd syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2985885012	Oculodental syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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