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123648007: Chromosomal alterations of group C and X (disorder)

Status: current, Defined. 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 Active Initial character case insensitive SNOMED CT core
726618011 Chromosomal alterations of group C and X (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

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 Associated morphology Congenital anomaly 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 Congenital anomaly 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 true Inferred relationship Some 1
Chromosomal alterations of group C and X Finding site Chromosome structure false Inferred relationship Some 1
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
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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