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

770669004: Paternal uniparental disomy of chromosome 5 (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
3701935011 Paternal uniparental disomy of chromosome 5 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3701936012 Paternal uniparental disomy of chromosome 5 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
Paternal uniparental disomy of chromosome 5 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Paternal uniparental disomy of chromosome 5 Finding site Chromosome pair 5 true Inferred relationship Existential restriction modifier 1
Paternal uniparental disomy of chromosome 5 Is a Uniparental disomy of paternal origin true Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 5 Is a Anomaly of chromosome pair 5 true Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 5 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