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715736008: Paternal uniparental disomy of chromosome 20 (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
3303565011 Paternal uniparental disomy of chromosome 20 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3303566012 Paternal uniparental disomy of chromosome 20 en Synonym Active Entire term case insensitive SNOMED CT core module
3303567015 Paternal UPD20 (uniparental disomy of chromosome 20) en Synonym 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 20 Is a Anomaly of chromosome pair 20 true Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 20 Is a Autosomal chromosomal disorder false Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 20 Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Paternal uniparental disomy of chromosome 20 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Paternal uniparental disomy of chromosome 20 Finding site Chromosome pair 20 true Inferred relationship Existential restriction modifier 1
Paternal uniparental disomy of chromosome 20 Is a Uniparental disomy of paternal origin true Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 20 Associated morphology Alteration of chromosome structure 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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