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15841002: 21q 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
26840010 21q partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
26841014 21q partial proximal monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
742746014 21q partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
26840010 21q partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
26840010 21q partial monosomy syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
26840010 21q partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
26841014 21q partial proximal monosomy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
26841014 21q partial proximal monosomy syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
26841014 21q partial proximal monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
742746014 21q partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
742746014 21q partial monosomy syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
742746014 21q partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
742746014 21q partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3452781001000114 Monosomie 21 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4441631000241117 monosomie partielle 21q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4441631000241117 monosomie partielle 21q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3452781001000114 Monosomie 21 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
21q partial monosomy syndrome (disorder) Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier (core metadata concept)
21q partial monosomy syndrome (disorder) Is a Anomaly of chromosome pair 21 false Inferred relationship Existential restriction modifier (core metadata concept)
21q partial monosomy syndrome (disorder) Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
21q partial monosomy syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
21q partial monosomy syndrome (disorder) Finding site Chromosome pair 21 false Inferred relationship Existential restriction modifier (core metadata concept) 1
21q partial monosomy syndrome (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
21q partial monosomy syndrome (disorder) Associated morphology Monosomy false Inferred relationship Existential restriction modifier (core metadata concept)
21q partial monosomy syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
21q partial monosomy syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
21q partial monosomy syndrome (disorder) Finding site Chromosome pair 21 false Inferred relationship Existential restriction modifier (core metadata concept) 1
21q partial monosomy syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
21q partial monosomy syndrome (disorder) Finding site Chromosome pair 21 true Inferred relationship Existential restriction modifier (core metadata concept) 1
21q partial monosomy syndrome (disorder) Associated morphology Deletion of long arm true Inferred relationship Existential restriction modifier (core metadata concept) 1
21q partial monosomy syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
21q partial monosomy syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
21q partial monosomy syndrome (disorder) Finding site Chromosome pair 21 true Inferred relationship Existential restriction modifier (core metadata concept) 2
21q partial monosomy syndrome (disorder) Is a Deletion of part of chromosome 21 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
21q22.11q22.12 microdeletion syndrome Is a True 21q partial monosomy syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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