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403760006: XXYY syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
1771686011 XXYY syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1782770018 XXYY syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
XXYY syndrome Is a Congenital disorder due to abnormality of chromosome number OR structure true Inferred relationship Existential restriction modifier
XXYY syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
XXYY syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
XXYY syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
XXYY syndrome Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
XXYY syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
XXYY syndrome Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
XXYY syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
XXYY syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
XXYY syndrome Finding site Chromosome structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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