71703005: Complete trisomy 22 syndrome (disorder)

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

\Disorder of foetus and/or newborn\Congenital disease\...

\Congenital malformation\Complete trisomy 22 syndrome (disorder)

\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 22\Trisomy 22\Complete trisomy 22 syndrome (disorder)
\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Trisomy 22\Complete trisomy 22 syndrome (disorder)

\Chromosomal disorder (disorder)\Autosomal chromosomal disorder (disorder)\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Trisomy 22\Complete trisomy 22 syndrome (disorder)
\Chromosomal disorder (disorder)\Duplication of chromosome (disorder)\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Trisomy 22\Complete trisomy 22 syndrome (disorder)
\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 22\Trisomy 22\Complete trisomy 22 syndrome (disorder)
\Chromosomal disorder (disorder)\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Trisomy 22\Complete trisomy 22 syndrome (disorder)

\Developmental disorder (disorder)\Congenital malformation\Complete trisomy 22 syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Complete trisomy 22 syndrome (disorder)	Is a	Anomaly of chromosome pair 22	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Complete trisomy 22 syndrome (disorder)	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Complete trisomy 22 syndrome (disorder)	Finding site	Chromosome pair 22	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Associated morphology	Trisomy (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Complete trisomy 22 syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Complete trisomy 22 syndrome (disorder)	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Complete trisomy 22 syndrome (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Finding site	Chromosome pair 22	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Complete trisomy 22 syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Finding site	Chromosome pair 22	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Associated morphology	Trisomy (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 22 syndrome (disorder)	Is a	Congenital malformation	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Complete trisomy 22 syndrome (disorder)	Is a	Trisomy 22	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
119117010	Complete trisomy 22 syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
811899018	Complete trisomy 22 syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
119117010	Complete trisomy 22 syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
119117010	Complete trisomy 22 syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
119118017	Antimongolism syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
811899018	Complete trisomy 22 syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
811899018	Complete trisomy 22 syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4624491000241115	trisomie totale 22	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4624491000241115	trisomie totale 22	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module