770629000: Distal 17p13.1 microdeletion 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 17\Deletion of part of short arm of chromosome 17\Distal 17p13.1 microdeletion syndrome
• \Anomaly of chromosome pair 17\Deletion of part of chromosome 17\Deletion of part of short arm of chromosome 17\Distal 17p13.1 microdeletion 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 17\Deletion of part of short arm of chromosome 17\Distal 17p13.1 microdeletion syndrome
• \Anomaly of chromosome pair 17\Deletion of part of chromosome 17\Deletion of part of short arm of chromosome 17\Distal 17p13.1 microdeletion syndrome

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
3701700017	Distal 17p13.1 microdeletion syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3701701018	Distal 17p13.1 microdeletion 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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