FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

1003873008: Uniparental disomy of paternal origin of chromosome 11 (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
4166866011 Paternal uniparental disomy of chromosome 11 en Synonym Active Entire term case insensitive SNOMED CT core module
4167332015 Uniparental disomy of paternal origin of chromosome 11 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4167333013 Uniparental disomy of paternal origin of chromosome 11 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 11 Is a Uniparental disomy of paternal origin true Inferred relationship Existential restriction modifier
Uniparental disomy of paternal origin of chromosome 11 Is a Anomaly of chromosome pair 11 true Inferred relationship Existential restriction modifier
Uniparental disomy of paternal origin of chromosome 11 Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier 1
Uniparental disomy of paternal origin of chromosome 11 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Uniparental disomy of paternal origin of chromosome 11 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

Back to Start