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70173007: 5p 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
116546014 5p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116547017 Cri du chat syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116548010 Lejeune syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116549019 5p minus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116550019 Partial deletion of short arm of chromosome 5 syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
810200013 5p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
116546014 5p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116546014 5p partial monosomy syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116546014 5p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116547017 Cri du chat syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116548010 Lejeune syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116549019 5p minus syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116549019 5p minus syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116549019 5p minus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116550019 Partial deletion of short arm of chromosome 5 syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116550019 Partial deletion of short arm of chromosome 5 syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
810200013 5p partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
810200013 5p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
810200013 5p partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
810200013 5p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1233229018 Deletion of short arm of chromosome 5 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1233229018 Deletion of short arm of chromosome 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3454091001000116 Cri-du-chat-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4619611000241117 monosomie partielle 5p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4619611000241117 monosomie partielle 5p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3454091001000116 Cri-du-chat-Syndrom 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
5p partial monosomy syndrome (disorder) Is a Anomaly of chromosome pair 5 (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Finding site Chromosome pair 5 false Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Associated morphology Monosomy false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Finding site Chromosome pair 5 false Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Finding site Chromosome pair 5 true Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
5p partial monosomy syndrome (disorder) Finding site Chromosome pair 5 false Inferred relationship Existential restriction modifier (core metadata concept) 2
5p partial monosomy syndrome (disorder) Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
5p partial monosomy syndrome (disorder) Is a Deletion of part of chromosome 5 (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
5p partial monosomy syndrome (disorder) Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier (core metadata concept) 2
5p partial monosomy syndrome (disorder) Is a Partial deletion of short arm of chromosome 5 true Inferred relationship Existential restriction modifier (core metadata concept)
5p partial monosomy syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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