733300002: Deletion of part of long arm of chromosome 17 (disorder)

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

\Disorder of foetus and/or newborn\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\...

\Monosomy and deletion from autosome (disorder)\Deletion of part of autosome\Deletion of part of chromosome 17\Deletion of part of long arm of chromosome 17

\Anomaly of chromosome pair 17 (disorder)\Deletion of part of chromosome 17\Deletion of part of long arm of chromosome 17

\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 17\Deletion of part of long arm of chromosome 17

\Anomaly of chromosome pair 17 (disorder)\Deletion of part of chromosome 17\Deletion of part of long arm of chromosome 17

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3499182011 Deletion of part of long arm of chromosome 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3499183018 Deletion of part of long arm of chromosome 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3499182011 Deletion of part of long arm of chromosome 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3499183018 Deletion of part of long arm of chromosome 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5927001000241117 délétion partielle du bras long du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5927011000241115 monosomie partielle du bras long du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5927021000241110 délétion partielle du chromosome 17q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5927001000241117 délétion partielle du bras long du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5927011000241115 monosomie partielle du bras long du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5927021000241110 délétion partielle du chromosome 17q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deletion of part of long arm of chromosome 17	Is a	Deletion of part of chromosome 17	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion of part of long arm of chromosome 17	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Deletion of part of long arm of chromosome 17	Finding site	Chromosome pair 17 (cell structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Deletion of part of long arm of chromosome 17	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Deletion of part of long arm of chromosome 17	Finding site	Chromosome pair 17 (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Deletion of part of long arm of chromosome 17	Associated morphology	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Deletion of part of long arm of chromosome 17	Associated morphology	Deletion of long arm	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Deletion of part of long arm of chromosome 17	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion of part of long arm of chromosome 17	Finding site	Long arm of chromosome (cell structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion of part of long arm of chromosome 17	Associated morphology	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
17q23.1q23.2 microdeletion syndrome (disorder)	Is a	True	Deletion of part of long arm of chromosome 17	Inferred relationship	Existential restriction modifier (core metadata concept)
Distal monosomy 17q (disorder)	Is a	True	Deletion of part of long arm of chromosome 17	Inferred relationship	Existential restriction modifier (core metadata concept)
17q12 microdeletion syndrome	Is a	True	Deletion of part of long arm of chromosome 17	Inferred relationship	Existential restriction modifier (core metadata concept)
17q11 deletion syndrome (disorder)	Is a	True	Deletion of part of long arm of chromosome 17	Inferred relationship	Existential restriction modifier (core metadata concept)
Proximal deletion of long arm of chromosome 17 (disorder)	Is a	True	Deletion of part of long arm of chromosome 17	Inferred relationship	Existential restriction modifier (core metadata concept)
17q24.2 microdeletion syndrome (disorder)	Is a	True	Deletion of part of long arm of chromosome 17	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets