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762271004: subklinische cystische fibrose (aandoening)


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
6267921000146115 subklinische cystische fibrose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267931000146118 subklinische cystische fibrose (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267941000146114 subklinische taaislijmziekte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267951000146112 subklinische CF nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6267961000146110 subklinische mucoviscidose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


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 Some
Subclinical cystic fibrosis Is a Cystic fibrosis true Inferred relationship Some
Subclinical cystic fibrosis Is a Hereditary disorder by system false Inferred relationship Some
Subclinical cystic fibrosis Has interpretation Impaired true Inferred relationship Some 2
Subclinical cystic fibrosis Interprets Mucociliary clearance true Inferred relationship Some 2
Subclinical cystic fibrosis Associated morphology defect false Inferred relationship Some 3
Subclinical cystic fibrosis Finding site Respiratory tract structure false Inferred relationship Some 3
Subclinical cystic fibrosis Finding site Respiratory tract structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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