123645005: Group chromosomal alteration (disorder)

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

\Disorder of foetus and/or newborn\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure (disorder)\Group chromosomal alteration

\Chromosomal disorder (disorder)\Congenital disorder due to abnormality of chromosome number OR structure (disorder)\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

1826611000005114 Ændring af kromosomgruppe da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Group chromosomal alteration	Is a	Anomaly of chromosome pair	false	Inferred relationship	Some
Group chromosomal alteration	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some	1
Group chromosomal alteration	Occurrence	Congenital	false	Inferred relationship	Some
Group chromosomal alteration	Finding site	Chromosome group	false	Inferred relationship	Some	1
Group chromosomal alteration	Is a	Congenital disorder due to abnormality of chromosome number OR structure (disorder)	true	Inferred relationship	Some
Group chromosomal alteration	Finding site	Chromosome structure	false	Inferred relationship	Some	2
Group chromosomal alteration	Associated morphology	kongenit anomali	false	Inferred relationship	Some	2
Group chromosomal alteration	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some	2
Group chromosomal alteration	Finding site	Chromosome group	true	Inferred relationship	Some	1
Group chromosomal alteration	Associated morphology	kongenit anomali	false	Inferred relationship	Some
Group chromosomal alteration	Finding site	Chromosome structure	false	Inferred relationship	Some	2
Group chromosomal alteration	Occurrence	Congenital	true	Inferred relationship	Some	1
Group chromosomal alteration	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1
Group chromosomal alteration	Finding site	Chromosome structure	false	Inferred relationship	Some	1

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

This concept is not in any reference sets