123645005: Group chromosomal alteration (disorder)

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

\Disorder of foetus and/or newborn\Congenital disease\Congenital chromosomal disease\Group chromosomal alteration

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Group chromosomal alteration

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

192134013 Group chromosomal alteration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

726615014 Group chromosomal alteration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

192134013 Group chromosomal alteration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

192134013 Group chromosomal alteration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

726615014 Group chromosomal alteration (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

726615014 Group chromosomal alteration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4767561000241116 altération d'un groupe chromosomique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4767561000241116 altération d'un groupe chromosomique 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
Group chromosomal alteration	Is a	Anomaly of chromosome pair	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Group chromosomal alteration	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Group chromosomal alteration	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Group chromosomal alteration	Finding site	Chromosome group	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Group chromosomal alteration	Is a	Congenital chromosomal disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Group chromosomal alteration	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Group chromosomal alteration	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Group chromosomal alteration	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Group chromosomal alteration	Finding site	Chromosome group	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Group chromosomal alteration	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Group chromosomal alteration	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Group chromosomal alteration	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Group chromosomal alteration	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Group chromosomal alteration	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Chromosomal alterations of group A	Is a	True	Group chromosomal alteration	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosomal alterations of group B	Is a	True	Group chromosomal alteration	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosomal alterations of group C and X	Is a	True	Group chromosomal alteration	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosomal alterations of group D	Is a	True	Group chromosomal alteration	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosomal alterations of group E (disorder)	Is a	True	Group chromosomal alteration	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosomal alterations of group F	Is a	True	Group chromosomal alteration	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosomal alterations of group G and Y	Is a	True	Group chromosomal alteration	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets