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1003871005: Uniparental disomy of paternal origin of chromosome 15 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4166863015 Paternal uniparental disomy of chromosome 15 en Synonym Active Entire term case insensitive SNOMED CT core module
4167336017 Uniparental disomy of paternal origin of chromosome 15 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4167337014 Uniparental disomy of paternal origin of chromosome 15 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
Uniparental disomy of paternal origin of chromosome 15 Is a Uniparental disomy of paternal origin true Inferred relationship Existential restriction modifier
Uniparental disomy of paternal origin of chromosome 15 Is a Anomaly of chromosome pair 15 true Inferred relationship Existential restriction modifier
Uniparental disomy of paternal origin of chromosome 15 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Uniparental disomy of paternal origin of chromosome 15 Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier 1
Uniparental disomy of paternal origin of chromosome 15 Finding site Chromosome pair 15 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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