403760006: XXYY syndrome (disorder)

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

\Chromosomal disorder (disorder)\Congenital chromosomal disease\XXYY syndrome (disorder)

\Congenital disease (disorder)\Congenital chromosomal disease\XXYY syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1771686011 XXYY syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

1782770018 XXYY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
XXYY syndrome (disorder)	Is a	Congenital chromosomal disease	true	Inferred relationship	Some
XXYY syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Some
XXYY syndrome (disorder)	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some
XXYY syndrome (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	1
XXYY syndrome (disorder)	Finding site	Chromosome structure	false	Inferred relationship	Some	1
XXYY syndrome (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Some
XXYY syndrome (disorder)	Finding site	Chromosome structure	false	Inferred relationship	Some	1
XXYY syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
XXYY syndrome (disorder)	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
XXYY syndrome (disorder)	Finding site	Chromosome structure	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets