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

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

Status: current, Primitive. 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	Active	Case insensitive	SNOMED CT core
829389018	Dominant autosomal hereditary disorder, incomplete penetrance (disorder)	en	Fully specified name	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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