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123650004: Chromosomal alterations of group E (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
192139015 Chromosomal alterations of group E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
726620014 Chromosomal alterations of group E (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
192139015 Chromosomal alterations of group E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
726620014 Chromosomal alterations of group E (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4767641000241118 altérations chromosomiques du groupe E fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4767641000241118 altérations chromosomiques du groupe E fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosomal alterations of group E (disorder) Is a Group chromosomal alteration true Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group E (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group E (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group E (disorder) Finding site Chromosomes, group E (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group E (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group E (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group E (disorder) Finding site Chromosomes, group E (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group E (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group E (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group E (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group E (disorder) Is a Congenital chromosomal disease false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group E (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group E (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group E (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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