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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
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
Uniparental disomy of paternal origin of chromosome 11 (disorder) Is a Uniparental disomy of paternal origin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Uniparental disomy of paternal origin of chromosome 11 (disorder) Is a Anomaly of chromosome pair 11 true Inferred relationship Existential restriction modifier (core metadata concept)
Uniparental disomy of paternal origin of chromosome 11 (disorder) Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Uniparental disomy of paternal origin of chromosome 11 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Uniparental disomy of paternal origin of chromosome 11 (disorder) Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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