205675007: individu met heterochromatine marker (aandoening)

SNOMED CT Concept\Clinical finding (finding)\Disease\Chromosomal disorder (disorder)\Balanced rearrangement and structural marker (disorder)\Individual with marker heterochromatin

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

315420015 Individual with marker heterochromatin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

591075011 Individual with marker heterochromatin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

11291131000146114 individu met heterochromatine marker nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

11291151000146115 individu met heterochromatine marker (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
Individual with marker heterochromatin	Is a	Balanced rearrangement and structural marker (disorder)	true	Inferred relationship	Some
Individual with marker heterochromatin	Occurrence	Congenital	false	Inferred relationship	Some
Individual with marker heterochromatin	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some
Individual with marker heterochromatin	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	1
Individual with marker heterochromatin	Finding site	Chromosome structure	false	Inferred relationship	Some	1
Individual with marker heterochromatin	Finding site	Chromosome structure	false	Inferred relationship	Some	1
Individual with marker heterochromatin	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some
Individual with marker heterochromatin	Finding site	Chromosome structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets