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726390009: Deletion of part of short arm of chromosome 17 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3464780015 Deletion of part of short arm of chromosome 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3464781016 Deletion of part of short arm of chromosome 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3464780015 Deletion of part of short arm of chromosome 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3464781016 Deletion of part of short arm of chromosome 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5855861000241112 délétion partielle du bras court du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5855871000241116 délétion d'une partie du bras court du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5855861000241112 délétion partielle du bras court du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5855871000241116 délétion d'une partie du bras court du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of short arm of chromosome 17 (disorder) Is a Deletion of part of chromosome 17 true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of short arm of chromosome 17 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Deletion of part of short arm of chromosome 17 (disorder) Finding site Chromosome pair 17 (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Deletion of part of short arm of chromosome 17 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Deletion of part of short arm of chromosome 17 (disorder) Finding site Chromosome pair 17 (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Deletion of part of short arm of chromosome 17 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Deletion of part of short arm of chromosome 17 (disorder) Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group
Distal 17p13.3 microdeletion syndrome Is a True Deletion of part of short arm of chromosome 17 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Distal 17p13.1 microdeletion syndrome Is a True Deletion of part of short arm of chromosome 17 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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