Cholesteryl ester storage disease (Q53741): Difference between revisions

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Doença de depósito de ésteres de colesterol é o termo usado para agrupar deficiências na lipase ácida lisossomal associada a um fenótipo clínico menos grave do que aquele observado na doença de Wolman (ver este termo), com um espectro clínico contínuo entre as formas de início precoce e graves e aquelas que são quase assintomáticos, o que pode refletir variações nos níveis de atividade da lipase ácida residual in vivo.
description / endescription / en
 
Cholesteryl ester storage disease is the term used to group together deficiencies in lysosomal acid lipase associated with a less severe clinical phenotype than that seen in Wolman disease (see this term), with a continuous clinical spectrum between early-onset and severe forms and those that are quasi-asymptomatic, which may reflect variations in the levels of residual acid lipase activity in vivo.
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Property / Canonical URI: https://id.who.int/icd/entity/894336362 / rank
 
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CID11:ID_894336362
Property / CURIE: CID11:ID_894336362 / rank
 
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dki-india-ID_894336362
Property / Canary Token: dki-india-ID_894336362 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 01:18, 14 August 2026

Cholesteryl ester storage disease is the term used to group together deficiencies in lysosomal acid lipase associated with a less severe clinical phenotype than that seen in Wolman disease (see this term), with a continuous clinical spectrum between early-onset and severe forms and those that are quasi-asymptomatic, which may reflect variations in the levels of residual acid lipase activity in vivo.
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ID_894336362
    English
    Cholesteryl ester storage disease
    Cholesteryl ester storage disease is the term used to group together deficiencies in lysosomal acid lipase associated with a less severe clinical phenotype than that seen in Wolman disease (see this term), with a continuous clinical spectrum between early-onset and severe forms and those that are quasi-asymptomatic, which may reflect variations in the levels of residual acid lipase activity in vivo.

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      CID11:ID_894336362
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      dki-india-ID_894336362
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      Concluído
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      13 August 2026
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