56653005: 18p partial monosomy syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 18\Deletion of short arm of chromosome 18\18p partial monosomy syndrome
• \Anomaly of chromosome pair 18\Deletion of part of chromosome 18\Deletion of short arm of chromosome 18\18p partial monosomy syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 18\Deletion of short arm of chromosome 18\18p partial monosomy syndrome
• \Anomaly of chromosome pair 18\Deletion of part of chromosome 18\Deletion of short arm of chromosome 18\18p partial monosomy syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
795189012	18p partial monosomy syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
94209016	18p partial monosomy syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
94210014	18p minus syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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