770411000: Distal monosomy 19p13.3 (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 19\Deletion of short arm of chromosome 19\Distal monosomy 19p13.3
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19\Deletion of short arm of chromosome 19\Distal monosomy 19p13.3
• \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 19\Deletion of short arm of chromosome 19\Distal monosomy 19p13.3
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19\Deletion of short arm of chromosome 19\Distal monosomy 19p13.3

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3700742012	Distal monosomy 19p13.3 (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3700744013	Distal monosomy 19p13.3	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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