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700285006: Congenital velopharyngeal dysfunction (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

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


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 Existential restriction modifier
Congenital velopharyngeal dysfunction Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital velopharyngeal dysfunction Is a Velopharyngeal inadequacy true Inferred relationship Existential restriction modifier
Congenital velopharyngeal dysfunction Finding site Muscle structure of pharynx true Inferred relationship Existential restriction modifier 2

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

This concept is not in any reference sets

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