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726384005: Deletion of part of chromosome 13 (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
3448837017 Deletion of part of chromosome 13 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448838010 Deletion of part of chromosome 13 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448837017 Deletion of part of chromosome 13 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448838010 Deletion of part of chromosome 13 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5996481000241114 monosomie partielle du chromosome 13 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996491000241111 délétion partielle du chromosome 13 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996481000241114 monosomie partielle du chromosome 13 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996491000241111 délétion partielle du chromosome 13 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

9 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 13 (disorder) Is a Anomaly of chromosome pair 13 true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 13 (disorder) Is a Deletion of part of autosome true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 13 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 13 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 13 (disorder) Finding site Chromosome pair 13 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
13q partial monosomy syndrome Is a False Deletion of part of chromosome 13 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Distal monosomy 13q syndrome Is a False Deletion of part of chromosome 13 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Distal deletion of chromosome 13 (disorder) Is a True Deletion of part of chromosome 13 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Medial deletion of chromosome 13 Is a True Deletion of part of chromosome 13 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of long arm of chromosome 13 (disorder) Is a True Deletion of part of chromosome 13 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Proximal deletion of chromosome 13 (disorder) Is a True Deletion of part of chromosome 13 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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