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123647002: Chromosomal alterations of group B (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
192136010 Chromosomal alterations of group B en Synonym Active Only initial character case insensitive SNOMED CT core module
726617018 Chromosomal alterations of group B (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 B Is a Group chromosomal alteration true Inferred relationship Existential restriction modifier
Chromosomal alterations of group B Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group B Finding site Chromosomes, group B true Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group B Occurrence Congenital false Inferred relationship Existential restriction modifier
Chromosomal alterations of group B Finding site Chromosome structure false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group B Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group B Finding site Chromosomes, group B false Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group B Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Chromosomal alterations of group B Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group B Finding site Chromosome structure false Inferred relationship Existential restriction modifier 2
Chromosomal alterations of group B Is a Congenital disorder due to abnormality of chromosome number OR structure false Inferred relationship Existential restriction modifier
Chromosomal alterations of group B Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group B Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Chromosomal alterations of group B 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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