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123646006: Chromosomal alterations of group A (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
192135014 Chromosomal alterations of group A en Synonym Active Only initial character case insensitive SNOMED CT core module
726616010 Chromosomal alterations of group A (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosomal alterations of group A Is a Group chromosomal alteration true Inferred relationship Existential restriction modifier
Chromosomal alterations of group A Finding site Chromosomes, group A true Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group A Occurrence Congenital false Inferred relationship Existential restriction modifier
Chromosomal alterations of group A Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group A Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group A Finding site Chromosome structure false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group A Finding site Chromosomes, group A false Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group A Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group A Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Chromosomal alterations of group A Finding site Chromosome structure false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group A Is a Congenital disorder due to abnormality of chromosome number OR structure false Inferred relationship Existential restriction modifier
Chromosomal alterations of group A Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group A Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group A Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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