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1003903008: Proximal deletion of long arm of chromosome 16 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4166929018 Proximal deletion of long arm of chromosome 16 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4166930011 Proximal deletion of long arm of chromosome 16 en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Proximal deletion of long arm of chromosome 16 Is a 16q partial monosomy syndrome false Inferred relationship Existential restriction modifier
Proximal deletion of long arm of chromosome 16 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Proximal deletion of long arm of chromosome 16 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Proximal deletion of long arm of chromosome 16 Finding site Chromosome pair 16 true Inferred relationship Existential restriction modifier 1
Proximal deletion of long arm of chromosome 16 Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 3
Proximal deletion of long arm of chromosome 16 Finding site Chromosome pair 16 false Inferred relationship Existential restriction modifier 3
Proximal deletion of long arm of chromosome 16 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Proximal deletion of long arm of chromosome 16 Is a Deletion of part of long arm of chromosome 16 true Inferred relationship Existential restriction modifier
Proximal deletion of long arm of chromosome 16 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Proximal deletion of long arm of chromosome 16 Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 2
Proximal deletion of long arm of chromosome 16 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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