FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

782691006: Maternal uniparental disomy of chromosome 21 (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
3755234019 Maternal uniparental disomy of chromosome 21 en Synonym Active Entire term case insensitive SNOMED CT core module
3755235018 Maternal uniparental disomy of chromosome 21 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3755236017 UPD(21)mat - maternal uniparental disomy of chromosome 21 en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Maternal uniparental disomy of chromosome 21 Is a Anomaly of chromosome pair 21 true Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 21 Finding site Chromosome pair 21 true Inferred relationship Existential restriction modifier 1
Maternal uniparental disomy of chromosome 21 Is a Uniparental disomy of maternal origin true Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 21 Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier 1
Maternal uniparental disomy of chromosome 21 Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start