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726392001: Deletion of part of chromosome 19 (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
3448853019 Deletion of part of chromosome 19 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448854013 Deletion of part of chromosome 19 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
10697441000172115 délétion d'une partie du chromosome 19 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
10697451000172118 délétion partielle du chromosome 19 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4239731000172118 partiële deletie van chromosoom 19 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4239741000172113 deletie van gedeelte van chromosoom 19 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 19 (disorder) Is a Anomaly of chromosome pair 19 true Inferred relationship Some
Deletion of part of chromosome 19 (disorder) Is a Deletion of part of autosome true Inferred relationship Some
Deletion of part of chromosome 19 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
Deletion of part of chromosome 19 (disorder) Occurrence Congenital true Inferred relationship Some 1
Deletion of part of chromosome 19 (disorder) Finding site Chromosome pair 19 true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
19p13.12 microdeletion syndrome (disorder) Is a False Deletion of part of chromosome 19 (disorder) Inferred relationship Some
19q13.11 microdeletion syndrome (disorder) Is a False Deletion of part of chromosome 19 (disorder) Inferred relationship Some
Deletion of long arm of chromosome 19 (disorder) Is a True Deletion of part of chromosome 19 (disorder) Inferred relationship Some
Deletion of short arm of chromosome 19 (disorder) Is a True Deletion of part of chromosome 19 (disorder) Inferred relationship Some
19p13.13 microdeletion syndrome (disorder) Is a False Deletion of part of chromosome 19 (disorder) Inferred relationship Some

This concept is not in any reference sets

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