897569003: Distal deletion of chromosome 15 (disorder)

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

\Disorder of foetus and/or newborn\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\...

\Monosomy and deletion from autosome (disorder)\Deletion of part of autosome\Deletion of part of chromosome 15 (disorder)\Distal deletion of chromosome 15 (disorder)

\Anomaly of chromosome pair 15\Deletion of part of chromosome 15 (disorder)\Distal deletion of chromosome 15 (disorder)

\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 15 (disorder)\Distal deletion of chromosome 15 (disorder)

\Anomaly of chromosome pair 15\Deletion of part of chromosome 15 (disorder)\Distal deletion of chromosome 15 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4034343012 Distal deletion of chromosome 15 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4034344018 Distal deletion of chromosome 15 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4034343012 Distal deletion of chromosome 15 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4034344018 Distal deletion of chromosome 15 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6087501000241111 délétion distale du chromosome 15 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6087501000241111 délétion distale du chromosome 15 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Distal deletion of chromosome 15 (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Distal deletion of chromosome 15 (disorder)	Finding site	Chromosome pair 15	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Distal deletion of chromosome 15 (disorder)	Is a	Deletion of part of chromosome 15 (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Distal deletion of chromosome 15 (disorder)	Associated morphology	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Distal monosomy 15q	Is a	True	Distal deletion of chromosome 15 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets