15q13.3 deletion (Q101710): Difference between revisions
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A síndrome da microdeleção 15q13.3 (microdel15q13.3) é caracterizada por um amplo espectro de transtornos do neurodesenvolvimento (atraso no desenvolvimento, principalmente na aquisição da fala, comprometimento cognitivo, epilepsia generalizada idiopática, transtornos neurocomportamentais do espectro autista ou psicótico), com nenhuma ou apenas sutis características dismórficas. | |||||||||||||||
| description / en | description / en | ||||||||||||||
15q13.3 microdeletion (microdel15q13.3) syndrome is characterised by a wide spectrum of neurodevelopmental disorders (developmental delay, mainly in speech acquisition, cognitive impairment, idiopathic generalised epilepsy, neurobehavioural disorders of the autistic or psychotic spectrum), with no or subtle dysmorphic features. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1824908852 / rank | |||||||||||||||
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CID11:ID_1824908852 | |||||||||||||||
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dki-india-ID_1824908852 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1824908852 / 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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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 18:33, 16 August 2026
15q13.3 microdeletion (microdel15q13.3) syndrome is characterised by a wide spectrum of neurodevelopmental disorders (developmental delay, mainly in speech acquisition, cognitive impairment, idiopathic generalised epilepsy, neurobehavioural disorders of the autistic or psychotic spectrum), with no or subtle dysmorphic features.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1824908852 |
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| English | 15q13.3 deletion |
15q13.3 microdeletion (microdel15q13.3) syndrome is characterised by a wide spectrum of neurodevelopmental disorders (developmental delay, mainly in speech acquisition, cognitive impairment, idiopathic generalised epilepsy, neurobehavioural disorders of the autistic or psychotic spectrum), with no or subtle dysmorphic features. |
Statements
CID11:ID_1824908852
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dki-india-ID_1824908852
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Concluído
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15 August 2026
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