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700285006: Congenital velopharyngeal dysfunction (disorder)


Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2989856013 Congenital velopharyngeal dysfunction (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2989902017 Congenital velopharyngeal dysfunction en Synonym Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital velopharyngeal dysfunction Is a Congenital disease true Inferred relationship Some
Congenital velopharyngeal dysfunction Occurrence Congenital true Inferred relationship Some 1
Congenital velopharyngeal dysfunction Is a Velopharyngeal inadequacy true Inferred relationship Some
Congenital velopharyngeal dysfunction Finding site Muscle structure of pharynx true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital velopharyngeal incompetence Is a True Congenital velopharyngeal dysfunction Inferred relationship Some

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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