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768471006: 16p12.2 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3685711016 16p12.2 microdeletion en Synonym Active Entire term case insensitive SNOMED CT core module
3685712011 16p12.2 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3685713018 16p12.2 microdeletion syndrome 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
16p12.2 microdeletion syndrome Finding site Chromosome pair 16 true Inferred relationship Existential restriction modifier 2
16p12.2 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
16p12.2 microdeletion syndrome Is a Deletion of part of short arm of chromosome 16 true Inferred relationship Existential restriction modifier
16p12.2 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
16p12.2 microdeletion syndrome Finding site Chromosome pair 16 false Inferred relationship Existential restriction modifier 1
16p12.2 microdeletion syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 1
16p12.2 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
16p12.2 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
16p12.2 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
16p12.2 microdeletion syndrome Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 1
16p12.2 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
16p12.2 microdeletion syndrome Associated morphology Partial monosomy true 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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