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427791009: Congenital velopharyngeal incompetence (disorder)


Status: current, Defined. 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 Case insensitive SNOMED CT core
2694181012 Congenital velopharyngeal incompetence en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Clinical finding foundation reference set

Respiratory finding reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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