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890394003: Congenital pulmonary airway malformation type 0 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4012457015 Congenital pulmonary airway malformation type 0 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4012458013 Congenital pulmonary airway malformation type 0 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4013156013 Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4012457015 Congenital pulmonary airway malformation type 0 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4012458013 Congenital pulmonary airway malformation type 0 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4013156013 Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5897141000241119 CPAM (congenital pulmonary airway malformation) de type 0 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5897151000241116 malformation adénomatoïde kystique du poumon de type 0 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5897161000241118 anomalie congénitale des voies aériennes pulmonaires de type 0 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5897141000241119 CPAM (congenital pulmonary airway malformation) de type 0 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5897151000241116 malformation adénomatoïde kystique du poumon de type 0 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5897161000241118 anomalie congénitale des voies aériennes pulmonaires de type 0 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
Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. Is a Congenital cystic adenomatoid malformation of lung true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. Associated morphology Cystic dilatation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. Finding site Lung structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pulmonary airway malformation type 0 originates in the trachea or bronchi with acinar dysgenesis, cartilage, smooth muscles, and glands separated by mesenchyme. It is fatal after birth. Pathological process (attribute) Pathological developmental process (qualifier value) 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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