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778073001: 3q26 microduplication syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3737638017 3q26 microduplication syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3737639013 Trisomy 3q26 en Synonym Active Entire term case insensitive SNOMED CT core module
3737640010 3q26 microduplication syndrome (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
3q26 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
3q26 microduplication syndrome Is a Partial trisomy of chromosome 3 true Inferred relationship Existential restriction modifier
3q26 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
3q26 microduplication syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
3q26 microduplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
3q26 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
3q26 microduplication syndrome Finding site Chromosome pair 3 true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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