123651000: verandering van chromosomenpaar 19 en 20 (aandoening)

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

\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital chromosomal disease\Group chromosomal alteration\Chromosomal alterations of group F

\Chromosomal disorder (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

9868271000146111 verandering van chromosoom van groep F nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9868321000146118 verandering van chromosomenpaar 19 en 20 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

10217831000146115 verandering van chromosomenpaar 19 en 20 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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	congenitale anomalie (afwijkende morfologie)	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	congenitale anomalie (afwijkende morfologie)	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