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427791009: Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (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
2694181012 Congenital velopharyngeal incompetence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5239120019 Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5239121015 Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2688893011 Congenital velopharyngeal incompetence (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5239120019 Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5239121015 Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3446451001000111 Velopharyngeale Funktionsstörungen, kongenitale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
157291000077118 insuffisance vélopharyngienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
902921000172111 incompétence vélopharyngienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
157291000077118 insuffisance vélopharyngienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
902921000172111 incompétence vélopharyngienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3446451001000111 Velopharyngeale Funktionsstörungen, kongenitale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Is a Velopharyngeal incompetence true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Finding site Muscle structure of pharynx false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Is a Congenital velopharyngeal dysfunction true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Finding site Muscle structure of pharynx false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Finding site Structure of velopharynx (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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