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726387003: Deletion of part of chromosome 16 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3448843015 Deletion of part of chromosome 16 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448844014 Deletion of part of chromosome 16 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448843015 Deletion of part of chromosome 16 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448844014 Deletion of part of chromosome 16 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5926971000241113 monosomie partielle du chromosome 16 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5926981000241110 délétion partielle du chromosome 16 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5926971000241113 monosomie partielle du chromosome 16 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5926981000241110 délétion partielle du chromosome 16 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 16 (disorder) Is a Anomaly of chromosome pair 16 true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 16 (disorder) Is a Deletion of part of autosome true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 16 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 16 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 16 (disorder) Finding site Chromosome pair 16 (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
16q partial monosomy syndrome Is a False Deletion of part of chromosome 16 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of short arm of chromosome 16 (disorder) Is a True Deletion of part of chromosome 16 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Partial deletion of long arm of chromosome 16 Is a True Deletion of part of chromosome 16 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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