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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
2467071000052116 kromosomförändringar, grupp C och X sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


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 Some
Chromosomal alterations of group C and X Occurrence Congenital false Inferred relationship Some
Chromosomal alterations of group C and X Finding site Chromosomes groups C and X false Inferred relationship Some 1
Chromosomal alterations of group C and X Associated morphology Alteration of chromosome structure false Inferred relationship Some 1
Chromosomal alterations of group C and X Associated morphology kongenital anomali false Inferred relationship Some 2
Chromosomal alterations of group C and X Finding site Chromosome structure false Inferred relationship Some 2
Chromosomal alterations of group C and X Finding site Chromosomes groups C and X true Inferred relationship Some 1
Chromosomal alterations of group C and X Associated morphology Alteration of chromosome structure false Inferred relationship Some 2
Chromosomal alterations of group C and X Associated morphology kongenital anomali false Inferred relationship Some
Chromosomal alterations of group C and X Finding site Chromosome structure false Inferred relationship Some 2
Chromosomal alterations of group C and X Is a Congenital chromosomal disease false Inferred relationship Some
Chromosomal alterations of group C and X Occurrence Congenital true Inferred relationship Some 1
Chromosomal alterations of group C and X Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Chromosomal alterations of group C and X Finding site Chromosome structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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