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783718003: Paternal uniparental disomy of chromosome X (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3759925010 Paternal uniparental disomy of chromosome X en Synonym Active Only initial character case insensitive SNOMED CT core module
3759926011 UPD(X)pat - paternal uniparental disomy of chromosome X en Synonym Active Entire term case sensitive SNOMED CT core module
3759927019 Paternal uniparental disomy of chromosome X (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Paternal uniparental disomy of chromosome X Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome X Is a Uniparental disomy of paternal origin true Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome X Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier 1
Paternal uniparental disomy of chromosome X Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Paternal uniparental disomy of chromosome X Finding site Sex chromosome X 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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