87006007: Dominant autosomal hereditary disorder, incomplete penetrance (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Dominant autosomal hereditary disorder, incomplete penetrance

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
144293012	Dominant autosomal hereditary disorder, incomplete penetrance	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
829389018	Dominant autosomal hereditary disorder, incomplete penetrance (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5865581000172115	maladie héréditaire autosomique dominante, pénétrance incomplète	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4476911000172118	autosomaal dominante erfelijke aandoening met incomplete penetrantie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4476921000172111	autosomaal dominante hereditaire aandoening met onvolledige penetrantie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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