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782669004: 10q22.3q23.3 microduplication syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3755079010 10q22.3q23.3 microduplication syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3755080013 10q22.3q23.3 microduplication syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3755081012 Trisomy 10q22.3q23.3 en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
10q22.3q23.3 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
10q22.3q23.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
10q22.3q23.3 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
10q22.3q23.3 microduplication syndrome Is a 10q partial trisomy syndrome true Inferred relationship Existential restriction modifier
10q22.3q23.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
10q22.3q23.3 microduplication syndrome Finding site Chromosome pair 10 true Inferred relationship Existential restriction modifier 2
10q22.3q23.3 microduplication syndrome Finding site Long arm of chromosome 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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