FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosomal alterations of group C and X est un(e) (attribut) Group chromosomal alteration true Inferred relationship Some
Chromosomal alterations of group C and X morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 2
Chromosomal alterations of group C and X localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 2
Chromosomal alterations of group C and X localisation d'une constatation (attribut) Chromosomes groups C and X true Inferred relationship Some 1
Chromosomal alterations of group C and X morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some 2
Chromosomal alterations of group C and X morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
Chromosomal alterations of group C and X localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 2
Chromosomal alterations of group C and X est un(e) (attribut) maladie chromosomique congénitale false Inferred relationship Some
Chromosomal alterations of group C and X survenue (attribut) congénital true Inferred relationship Some 1
Chromosomal alterations of group C and X morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Chromosomal alterations of group C and X localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
Chromosomal alterations of group C and X survenue (attribut) congénital false Inferred relationship Some
Chromosomal alterations of group C and X localisation d'une constatation (attribut) Chromosomes groups C and X false Inferred relationship Some 1
Chromosomal alterations of group C and X morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

Back to Start