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726365007: Deletion of part of chromosome 1 (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
3448799012 Deletion of part of chromosome 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448800011 Deletion of part of chromosome 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448799012 Deletion of part of chromosome 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448800011 Deletion of part of chromosome 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6016541000241110 délétion partielle du chromosome 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6016551000241113 monosomie partielle du chromosome 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6016541000241110 délétion partielle du chromosome 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6016551000241113 monosomie partielle du chromosome 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

15 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 1 (disorder) Is a Anomaly of chromosome pair 1 true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 1 (disorder) Is a Deletion of part of autosome true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 1 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 1 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 1 (disorder) Finding site Chromosome pair 1 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
1q partial monosomy (disorder) Is a True Deletion of part of chromosome 1 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
1p partial monosomy Is a True Deletion of part of chromosome 1 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
1p36 deletion syndrome Is a False Deletion of part of chromosome 1 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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