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472825005: Fetal chromosomal abnormality screening (procedure)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2013. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2951925011 Foetal chromosomal abnormality screening en Synonym Active Entire term case insensitive SNOMED CT core module
2951931014 Fetal chromosomal abnormality screening en Synonym Active Entire term case insensitive SNOMED CT core module
2951938015 Fetal chromosomal abnormality screening (procedure) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fetal chromosomal abnormality screening Is a Chromosome abnormality screening true Inferred relationship Existential restriction modifier
Fetal chromosomal abnormality screening Method Evaluation - action true Inferred relationship Existential restriction modifier 1
Fetal chromosomal abnormality screening Has intent Screening - procedure intent true Inferred relationship Existential restriction modifier 2
Fetal chromosomal abnormality screening Has focus Chromosomal disorder true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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