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762270003: Atypical 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
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
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
5498841000241117 mucoviscidose atypique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5498841000241117 mucoviscidose atypique 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
Atypical cystic fibrosis (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Atypical cystic fibrosis (disorder) Is a Cystic fibrosis true Inferred relationship Existential restriction modifier (core metadata concept)
Atypical cystic fibrosis (disorder) Is a Hereditary disorder by system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Atypical cystic fibrosis (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Atypical cystic fibrosis (disorder) Interprets Mucociliary clearance true Inferred relationship Existential restriction modifier (core metadata concept) 2
Atypical cystic fibrosis (disorder) Associated morphology Defect false Inferred relationship Existential restriction modifier (core metadata concept) 3
Atypical cystic fibrosis (disorder) Finding site Respiratory tract structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Atypical cystic fibrosis (disorder) 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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