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719650004: 20p12.3 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3317243015 20p12.3 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3317244014 20p12.3 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3317245010 Monosomy 20p12.3 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
20p12.3 microdeletion syndrome Is a Anomaly of chromosome pair 20 false Inferred relationship Existential restriction modifier
20p12.3 microdeletion syndrome Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier
20p12.3 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
20p12.3 microdeletion syndrome Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 2
20p12.3 microdeletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
20p12.3 microdeletion syndrome Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 3
20p12.3 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
20p12.3 microdeletion syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 3
20p12.3 microdeletion syndrome Is a Deletion of part of short arm of chromosome 20 true Inferred relationship Existential restriction modifier
20p12.3 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
20p12.3 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
20p12.3 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
20p12.3 microdeletion syndrome Finding site Chromosome pair 20 true Inferred relationship Existential restriction modifier 1
20p12.3 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
20p12.3 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
20p12.3 microdeletion syndrome Finding site Short arm of chromosome 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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