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766816008: 2q23.1 microduplication syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3662714013 2q23.1 microduplication syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3662715014 2q23.1 microduplication syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3662716010 Trisomy 2q23.1 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
2q23.1 microduplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
2q23.1 microduplication syndrome Finding site Chromosome pair 2 true Inferred relationship Existential restriction modifier 1
2q23.1 microduplication syndrome Is a 2q partial trisomy syndrome true Inferred relationship Existential restriction modifier
2q23.1 microduplication syndrome Associated morphology Partial trisomy 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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