Congenital aortic valvar stenosis (Q46201): Difference between revisions

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Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1824398514 / rank
 
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Property / CURIE
 
CID11:LA8A.20
Property / CURIE: CID11:LA8A.20 / rank
 
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Property / Canary Token
 
dki-india-LA8A.20
Property / Canary Token: dki-india-LA8A.20 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: Q23.0 / rank
 
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Latest revision as of 14:37, 13 August 2026

A congenital cardiovascular malformation of the aortic valve in which there is narrowing or stricture (obstruction to flow). Additional information: 'Congenital aortic valvar stenosis' arises most commonly as a result of partial or complete fusion of one or more commissures, or is due to dysplasia of one or more aortic cusps. These congenital malformations of the aortic valve may not be initially obstructive but may become stenotic later in life due to leaflet thickening, poor relative growth and-or calcification. It is not until the congenitally malformed aortic valve is or becomes stenotic that this term should be used.
Language Label Description Also known as
default for all languages
LA8A.20
    English
    Congenital aortic valvar stenosis
    A congenital cardiovascular malformation of the aortic valve in which there is narrowing or stricture (obstruction to flow). Additional information: 'Congenital aortic valvar stenosis' arises most commonly as a result of partial or complete fusion of one or more commissures, or is due to dysplasia of one or more aortic cusps. These congenital malformations of the aortic valve may not be initially obstructive but may become stenotic later in life due to leaflet thickening, poor relative growth and-or calcification. It is not until the congenitally malformed aortic valve is or becomes stenotic that this term should be used.

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      CID11:LA8A.20
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      dki-india-LA8A.20
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      Concluído
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      13 August 2026
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