880081006: 12q15 deletion syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\...

\Monosomy and deletion from autosome (disorder)\Deletion of part of autosome\Deletion of part of chromosome 12 (disorder)\Deletion of part of long arm of chromosome 12 (disorder)\12q15 deletion syndrome (disorder)

\Anomaly of chromosome pair 12\Deletion of part of chromosome 12 (disorder)\Deletion of part of long arm of chromosome 12 (disorder)\12q15 deletion syndrome (disorder)

\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\12q15 deletion syndrome (disorder)
\Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome (disorder)\Deletion of part of autosome\Deletion of part of chromosome 12 (disorder)\Deletion of part of long arm of chromosome 12 (disorder)\12q15 deletion syndrome (disorder)
\Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 12\Deletion of part of chromosome 12 (disorder)\Deletion of part of long arm of chromosome 12 (disorder)\12q15 deletion syndrome (disorder)

\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\12q15 deletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3994443012 12q15 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3994444018 12q15 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4844531000052114 12q15-deletionssyndromet sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
12q15 deletion syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
12q15 deletion syndrome (disorder)	Is a	Deletion of part of long arm of chromosome 12 (disorder)	true	Inferred relationship	Some
12q15 deletion syndrome (disorder)	Associated morphology	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Some	1
12q15 deletion syndrome (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
12q15 deletion syndrome (disorder)	Finding site	Chromosome pair 12	true	Inferred relationship	Some	1
12q15 deletion syndrome (disorder)	Associated morphology	Deletion of long arm	false	Inferred relationship	Some	2
12q15 deletion syndrome (disorder)	Finding site	Chromosome pair 12	false	Inferred relationship	Some	2
12q15 deletion syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
12q15 deletion syndrome (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
12q15 deletion syndrome (disorder)	Is a	Multiple system malformation syndrome	true	Inferred relationship	Some
12q15 deletion syndrome (disorder)	Finding site	Long arm of chromosome	true	Inferred relationship	Some	2
12q15 deletion syndrome (disorder)	Associated morphology	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
12q15q21.1 microdeletion syndrome (disorder)	Is a	False	12q15 deletion syndrome (disorder)	Inferred relationship	Some

Reference Sets