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

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
144293012 Dominant autosomal hereditary disorder, incomplete penetrance en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
4674651000241111 maladie héréditaire autosomique dominante, pénétrance incomplète fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4674651000241111 maladie héréditaire autosomique dominante, pénétrance incomplète fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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 Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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