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87006007: autosomaal dominante hereditaire aandoening met onvolledige penetrantie (aandoening)


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
6357311000146114 autosomaal dominante hereditaire aandoening met onvolledige penetrantie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6357321000146116 autosomaal dominante hereditaire aandoening met onvolledige penetrantie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6357331000146119 autosomaal dominante erfelijke aandoening met incomplete penetrantie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dominant autosomal hereditary disorder, incomplete penetrance Is a Autosomal dominant hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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