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726391008: Deletion of part of chromosome 18 (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
3448851017 Deletion of part of chromosome 18 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448852012 Deletion of part of chromosome 18 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448851017 Deletion of part of chromosome 18 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448852012 Deletion of part of chromosome 18 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5846221000241110 délétion d'une partie du chromosome 18 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5846231000241112 délétion partielle du chromosome 18 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5846221000241110 délétion d'une partie du chromosome 18 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5846231000241112 délétion partielle du chromosome 18 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

7 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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