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56653005: 18p partial monosomy syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
94209016 18p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
94210014 18p minus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
795189012 18p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
94209016 18p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
94209016 18p partial monosomy syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
94209016 18p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
94210014 18p minus syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
94210014 18p minus syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
94210014 18p minus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
795189012 18p partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
795189012 18p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
795189012 18p partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
795189012 18p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3392001001000118 Monosomie 18p de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4575691000241112 monosomie partielle 18p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4575691000241112 monosomie partielle 18p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3392001001000118 Monosomie 18p de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
18p partial monosomy syndrome Is a Anomaly of chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Associated morphology Monosomy false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
18p partial monosomy syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
18p partial monosomy syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
18p partial monosomy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
18p partial monosomy syndrome Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier (core metadata concept) 1
18p partial monosomy syndrome Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier (core metadata concept) 1
18p partial monosomy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
18p partial monosomy syndrome Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
18p partial monosomy syndrome Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier (core metadata concept) 2
18p partial monosomy syndrome Is a Deletion of part of chromosome 18 (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
18p partial monosomy syndrome Is a Deletion of short arm of chromosome 18 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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