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427791009: Congenital velopharyngeal incompetence (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2688893011 Congenital velopharyngeal incompetence (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2694181012 Congenital velopharyngeal incompetence en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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