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24786004: 7p partial monosomy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4571150017 7p partial monosomy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4571151018 7p partial monosomy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
41537012 7p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
41537012 7p partial monosomy syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
41537012 7p partial monosomy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
754461018 7p partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
754461018 7p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
754461018 7p partial monosomy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
754461018 7p partial monosomy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4571150017 7p partial monosomy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4571151018 7p partial monosomy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4470151000241110 monosomie partielle 7p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4470151000241110 monosomie partielle 7p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
7p partial monosomy Is a Anomaly of chromosome pair 7 false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Finding site Chromosome pair 7 false Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Associated morphology Monosomy false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Finding site Chromosome pair 7 false Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Finding site Chromosome pair 7 false Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
7p partial monosomy Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
7p partial monosomy Finding site Chromosome pair 7 true Inferred relationship Existential restriction modifier (core metadata concept) 2
7p partial monosomy Is a Deletion of part of chromosome 7 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
7p partial monosomy Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
7p partial monosomy Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier (core metadata concept) 2
7p partial monosomy Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
7p partial monosomy Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Distal monosomy 7p syndrome (disorder) Is a True 7p partial monosomy Inferred relationship Existential restriction modifier (core metadata concept)
7p12-p14 deletion syndrome Is a True 7p partial monosomy Inferred relationship Existential restriction modifier (core metadata concept)
7p21.1 deletion syndrome (disorder) Is a True 7p partial monosomy Inferred relationship Existential restriction modifier (core metadata concept)
Proximal deletion of short arm of chromosome 7 (disorder) Is a True 7p partial monosomy Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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