726380001: Deletion of part of chromosome 10 (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\...

\Monosomy and deletion from autosome (disorder)\Deletion of part of autosome\Deletion of part of chromosome 10 (disorder)

\Anomaly of chromosome pair 10\Deletion of part of chromosome 10 (disorder)

\Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\...

\Monosomy and deletion from autosome (disorder)\Deletion of part of autosome\Deletion of part of chromosome 10 (disorder)

\Anomaly of chromosome pair 10\Deletion of part of chromosome 10 (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

3448829013 Deletion of part of chromosome 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3448830015 Deletion of part of chromosome 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

10697171000172117 délétion d'une partie du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

10697181000172119 délétion partielle du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4867461000172111 partiële deletie van chromosoom 10 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4867471000172119 deletie van gedeelte van chromosoom 10 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deletion of part of chromosome 10 (disorder)	Is a	Anomaly of chromosome pair 10	true	Inferred relationship	Some
Deletion of part of chromosome 10 (disorder)	Is a	Deletion of part of autosome	true	Inferred relationship	Some
Deletion of part of chromosome 10 (disorder)	Associated morphology	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Some	1
Deletion of part of chromosome 10 (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Deletion of part of chromosome 10 (disorder)	Finding site	Chromosome pair 10 (cell structure)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
10p partial monosomy syndrome	Is a	True	Deletion of part of chromosome 10 (disorder)	Inferred relationship	Some
10q partial monosomy (disorder)	Is a	True	Deletion of part of chromosome 10 (disorder)	Inferred relationship	Some

This concept is not in any reference sets