274908005: Deletion with complex rearrangement (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 with complex rearrangement

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome (disorder)\Deletion with complex rearrangement

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

410807013 Deletion with complex rearrangement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

667717015 Deletion with complex rearrangement (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

410807013 Deletion with complex rearrangement en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

410807013 Deletion with complex rearrangement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

667717015 Deletion with complex rearrangement (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

667717015 Deletion with complex rearrangement (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5117801000241119 délétion avec réarrangement complexe fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5117801000241119 délétion avec réarrangement complexe 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
Deletion with complex rearrangement	Is a	Monosomy and deletion from autosome (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion with complex rearrangement	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion with complex rearrangement	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion with complex rearrangement	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion with complex rearrangement	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion with complex rearrangement	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion with complex rearrangement	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion with complex rearrangement	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion with complex rearrangement	Associated morphology	Cellular AND/OR subcellular abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion with complex rearrangement	Finding site	Chromosome	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Deletions with other complex rearrangements	Is a	False	Deletion with complex rearrangement	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets