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205666005: Duplication with other complex rearrangement (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
315409015 Duplication with other complex rearrangement en Synonym Active Entire term case insensitive SNOMED CT core module
591065013 Duplication with other complex rearrangement (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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