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1003873008: Uniparental disomy of paternal origin of chromosome 11 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4166866011 Paternal uniparental disomy of chromosome 11 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4167332015 Uniparental disomy of paternal origin of chromosome 11 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4167333013 Uniparental disomy of paternal origin of chromosome 11 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Paternal uniparental disomy of chromosome 11 Is a Uniparental disomy of paternal origin (disorder) true Inferred relationship Some
Paternal uniparental disomy of chromosome 11 Is a Anomaly of chromosome pair 11 (disorder) true Inferred relationship Some
Paternal uniparental disomy of chromosome 11 Finding site Chromosome pair 11 true Inferred relationship Some 1
Paternal uniparental disomy of chromosome 11 Occurrence Congenital true Inferred relationship Some 1
Paternal uniparental disomy of chromosome 11 Associated morphology Alteration of chromosome structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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