123651000: Chromosomal alterations of group F (disorder)

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

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Group chromosomal alteration\Chromosomal alterations of group F

\Congenital disease (disorder)\Congenital chromosomal disease\Group chromosomal alteration\Chromosomal alterations of group F

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

4767661000241117 altérations chromosomiques du groupe F fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chromosomal alterations of group F	Is a	Group chromosomal alteration	true	Inferred relationship	Some
Chromosomal alterations of group F	Occurrence	Congenital	false	Inferred relationship	Some
Chromosomal alterations of group F	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some	1
Chromosomal alterations of group F	Finding site	Chromosomes, group F	true	Inferred relationship	Some	1
Chromosomal alterations of group F	Finding site	Chromosome structure	false	Inferred relationship	Some	2
Chromosomal alterations of group F	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	2
Chromosomal alterations of group F	Finding site	Chromosomes, group F	false	Inferred relationship	Some	1
Chromosomal alterations of group F	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some	2
Chromosomal alterations of group F	Associated morphology	anomalie congénitale	false	Inferred relationship	Some
Chromosomal alterations of group F	Finding site	Chromosome structure	false	Inferred relationship	Some	2
Chromosomal alterations of group F	Is a	Congenital chromosomal disease	false	Inferred relationship	Some
Chromosomal alterations of group F	Occurrence	Congenital	true	Inferred relationship	Some	1
Chromosomal alterations of group F	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Chromosomal alterations of group F	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