123651000: Chromosomal alterations of group F (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 alterations of group F (disorder)

\Chromosomal disorder (disorder)\Congenital disorder due to abnormality of chromosome number OR structure (disorder)\Group chromosomal alteration\Chromosomal alterations of group F (disorder)

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

192140018 Chromosomal alterations of group F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

726622018 Chromosomal alterations of group F (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1826671000005119 Ændring af kromosomgruppe F da Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets