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762270003: atypische 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
3636281015 Atypical cystic fibrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636282010 Atypical cystic fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6187181000146116 atypische cystische fibrose (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6187191000146119 atypische CF nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6187201000146117 atypische mucoviscidose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6187211000146115 atypische cystische fibrose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6187221000146113 atypische taaislijmziekte 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
Atypical cystic fibrosis (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Atypical cystic fibrosis (disorder) Is a Cystic fibrosis true Inferred relationship Some
Atypical cystic fibrosis (disorder) Is a Hereditary disorder by system false Inferred relationship Some
Atypical cystic fibrosis (disorder) Has interpretation Impaired true Inferred relationship Some 2
Atypical cystic fibrosis (disorder) Interprets Mucociliary clearance true Inferred relationship Some 2
Atypical cystic fibrosis (disorder) Associated morphology defect false Inferred relationship Some 3
Atypical cystic fibrosis (disorder) Finding site Respiratory tract structure false Inferred relationship Some 3
Atypical cystic fibrosis (disorder) 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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