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123648007: Chromosomal alterations of group C and X (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
192137018 Chromosomal alterations of group C and X en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
726618011 Chromosomal alterations of group C and X (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
192137018 Chromosomal alterations of group C and X en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
726618011 Chromosomal alterations of group C and X (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5741371000241111 altérations chromosomiques des groupes C et X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5741381000241113 altérations des chromosomes de 6 à 12 et du chromosome X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5741371000241111 altérations chromosomiques des groupes C et X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5741381000241113 altérations des chromosomes de 6 à 12 et du chromosome X 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 C and X Is a Group chromosomal alteration true Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group C and X Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group C and X Finding site Chromosomes groups C and X false Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group C and X Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group C and X Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group C and X Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group C and X Finding site Chromosomes groups C and X true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group C and X Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group C and X Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group C and X Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chromosomal alterations of group C and X Is a Congenital chromosomal disease false Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal alterations of group C and X Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group C and X Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosomal alterations of group C and X 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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