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762271004: Subclinical cystic fibrosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3636283017 Subclinical cystic fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636284011 Subclinical cystic fibrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636283017 Subclinical cystic fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636284011 Subclinical cystic fibrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5498861000241116 mucoviscidose subclinique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5498861000241116 mucoviscidose subclinique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Subclinical cystic fibrosis Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Subclinical cystic fibrosis Is a Cystic fibrosis true Inferred relationship Existential restriction modifier (core metadata concept)
Subclinical cystic fibrosis Is a Hereditary disorder by system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Subclinical cystic fibrosis Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Subclinical cystic fibrosis Interprets Mucociliary clearance true Inferred relationship Existential restriction modifier (core metadata concept) 2
Subclinical cystic fibrosis Associated morphology Defect false Inferred relationship Existential restriction modifier (core metadata concept) 3
Subclinical cystic fibrosis Finding site Respiratory tract structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Subclinical cystic fibrosis Finding site Respiratory tract 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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