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427791009: Congenital velopharyngeal incompetence (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2008. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2688893011 Congenital velopharyngeal incompetence (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2694181012 Congenital velopharyngeal incompetence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1474731000052119 medfödd velofaryngeal insufficiens sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital velopharyngeal incompetence (disorder) Is a Velopharyngeal incompetence false Inferred relationship Some
Congenital velopharyngeal incompetence (disorder) Is a Congenital disease (disorder) false Inferred relationship Some
Congenital velopharyngeal incompetence (disorder) Finding site Muscle structure of pharynx false Inferred relationship Some
Congenital velopharyngeal incompetence (disorder) Occurrence Congenital false Inferred relationship Some
Congenital velopharyngeal incompetence (disorder) Is a Congenital velopharyngeal dysfunction (disorder) true Inferred relationship Some
Congenital velopharyngeal incompetence (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital velopharyngeal incompetence (disorder) Finding site Muscle structure of pharynx 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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