1003449005: Paternal 14q32.2 microdeletion (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 14\Partial deletion of long arm of chromosome 14\Paternal 14q32.2 microdeletion
• \Anomaly of chromosome pair 14\Deletion of part of chromosome 14\Partial deletion of long arm of chromosome 14\Paternal 14q32.2 microdeletion
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 14\Partial deletion of long arm of chromosome 14\Paternal 14q32.2 microdeletion
• \Anomaly of chromosome pair 14\Deletion of part of chromosome 14\Partial deletion of long arm of chromosome 14\Paternal 14q32.2 microdeletion

Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4164743018	Paternal 14q32.2 microdeletion (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4164744012	Paternal 14q32.2 microdeletion	en	Synonym	Active	Case insensitive	SNOMED CT core
4164745013	Paternal monosomy 14q32.2	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start