764739008: Proximal chromosome 18q deletion syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 18\Deletion of long arm of chromosome 18\18q partial monosomy syndrome\Proximal chromosome 18q deletion syndrome
• \Anomaly of chromosome pair 18\Deletion of part of chromosome 18\Deletion of long arm of chromosome 18\18q partial monosomy syndrome\Proximal chromosome 18q deletion syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 18\Deletion of long arm of chromosome 18\18q partial monosomy syndrome\Proximal chromosome 18q deletion syndrome
• \Anomaly of chromosome pair 18\Deletion of part of chromosome 18\Deletion of long arm of chromosome 18\18q partial monosomy syndrome\Proximal chromosome 18q deletion syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3654946017	Proximal chromosome 18q deletion syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3654947014	Proximal chromosome 18q deletion syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3654948016	Proximal 18q deletion syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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