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726706008: 4p16.3 microduplication syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3451922019 4p16.3 microduplication syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3451923012 4p16.3 microduplication syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3451924018 Distal trisomy 4p en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
4p16.3 microduplication syndrome Is a 4p partial trisomy syndrome true Inferred relationship Existential restriction modifier
4p16.3 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
4p16.3 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
4p16.3 microduplication syndrome Finding site Chromosome pair 4 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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