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1003870006: Uniparental disomy of paternal origin of chromosome 4 (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
4166860017 Paternal uniparental disomy of chromosome 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4167327016 Uniparental disomy of paternal origin of chromosome 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4167328014 Uniparental disomy of paternal origin of chromosome 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
7694251000241112 disomie uniparentale du chromosome 4, d'origine paternelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Paternal uniparental disomy of chromosome 4 Is a Anomaly of chromosome pair 4 true Inferred relationship Some
Paternal uniparental disomy of chromosome 4 Is a Uniparental disomy of paternal origin (disorder) true Inferred relationship Some
Paternal uniparental disomy of chromosome 4 Occurrence Congenital true Inferred relationship Some 1
Paternal uniparental disomy of chromosome 4 Finding site Chromosome pair 4 (cell structure) true Inferred relationship Some 1
Paternal uniparental disomy of chromosome 4 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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