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718128009: Congenital dysplasia of cardiac valve (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3311244016 Congenital dysplasia of cardiac valve (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311245015 Congenital dysplasia of cardiac valve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311246019 Congenital valvular dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311244016 Congenital dysplasia of cardiac valve (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311244016 Congenital dysplasia of cardiac valve (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311245015 Congenital dysplasia of cardiac valve en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311245015 Congenital dysplasia of cardiac valve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311246019 Congenital valvular dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311246019 Congenital valvular dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311247011 A rare entity usually diagnosed by echocardiography. It may be limited to one of the four valves but can also involve the two atrioventricular valves and the two semilunar valves. May be the hallmark of genetic anomalies. Chromosomal anomalies should be searched when polyvalvular dysplasia is found in a fetus, namely trisomy 18 and trisomy 13. Triscuspid valve dysplasia can be the only cardiac finding in trisomy 21 and a karyotype analysis should be performed in all fetuses exhibiting this anomaly. In the absence of chromosomal anomalies, polyvalvular dysplasia can be observed in Noonan syndrome. Thickening of the different cardiac valves can be observed in various storage diseases such as mucopolysaccharidoses. In these later conditions, it develops after the neonatal period and is frequently associated with extracardiac symptoms suggestive of the diagnosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5478761000241117 dysplasie congénitale d'une valve cardiaque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5478761000241117 dysplasie congénitale d'une valve cardiaque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital dysplasia of cardiac valve (disorder) Is a Congenital anomaly of heart valve (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dysplasia of cardiac valve (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dysplasia of cardiac valve (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dysplasia of cardiac valve (disorder) Finding site Cardiac valve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dysplasia of cardiac valve (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dysplasia of cardiac valve (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Mitral valve dysplasia Is a True Congenital dysplasia of cardiac valve (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Truncal valve dysplasia Is a False Congenital dysplasia of cardiac valve (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary valve dysplasia (disorder) Is a True Congenital dysplasia of cardiac valve (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Polyvalvular heart disease syndrome (disorder) Is a True Congenital dysplasia of cardiac valve (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dysplasia of aortic valve (disorder) Is a True Congenital dysplasia of cardiac valve (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dysplasia of truncal valve Is a True Congenital dysplasia of cardiac valve (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dysplasia of tricuspid valve (disorder) Is a True Congenital dysplasia of cardiac valve (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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