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700285006: Congenital incomplete closure of velopharyngeal apparatus (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
2989902017 Congenital velopharyngeal dysfunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5223482015 Congenital incomplete closure of velopharyngeal apparatus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5223483013 Congenital velopharyngeal inadequacy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5223484019 Congenital incomplete closure of velopharyngeal apparatus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2989856013 Congenital velopharyngeal dysfunction (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2989856013 Congenital velopharyngeal dysfunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2989902017 Congenital velopharyngeal dysfunction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2989902017 Congenital velopharyngeal dysfunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5223482015 Congenital incomplete closure of velopharyngeal apparatus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5223483013 Congenital velopharyngeal inadequacy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5223484019 Congenital incomplete closure of velopharyngeal apparatus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5440661000241112 dysfonction vélopharyngée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5440661000241112 dysfonction vélopharyngée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 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 (core metadata concept)
Congenital velopharyngeal dysfunction Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital velopharyngeal dysfunction Is a Velopharyngeal dysfunction true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital velopharyngeal dysfunction Finding site Muscle structure of pharynx false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital velopharyngeal dysfunction Is a Developmental disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital velopharyngeal dysfunction Finding site Muscle structure of pharynx false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital velopharyngeal dysfunction Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital velopharyngeal dysfunction Is a Respiratory condition of fetus OR newborn false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital velopharyngeal dysfunction Is a Disorder of digestive system specific to fetus OR newborn true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital velopharyngeal dysfunction 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
Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction (disorder) Is a True Congenital velopharyngeal dysfunction Inferred relationship Existential restriction modifier (core metadata concept)
Congenital incomplete closure of velopharyngeal apparatus due to anatomical abnormality (disorder) Is a True Congenital velopharyngeal dysfunction Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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