Distal 17q deletion (Q101727): Difference between revisions

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A síndrome da deleção do cromossomo 17q (deleção do braço longo do cromossomo 17) é um transtorno cromossômico muito raro caracterizado por múltiplas anormalidades craniofaciais (microcefalia e deformidades de olhos, orelhas e nariz), de membros e outras anormalidades de múltiplos órgãos, retardo de crescimento e motor, e déficit intelectual . A síndrome é frequentemente letal.
description / endescription / en
 
Chromosome 17q deletion syndrome (deletion of the long arm of chromosome 17) is a very rare chromosomal disorder characterised by multiple craniofacial (microcephaly and eye, ear, and nose deformities), limb and other multiple organ abnormalities, growth and motor retardation and intellectual deficit. The syndrome is frequently lethal.
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Property / Canonical URI: https://id.who.int/icd/entity/19213480 / rank
 
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CID11:ID_19213480
Property / CURIE: CID11:ID_19213480 / rank
 
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dki-india-ID_19213480
Property / Canary Token: dki-india-ID_19213480 / 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
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 18:34, 16 August 2026

Chromosome 17q deletion syndrome (deletion of the long arm of chromosome 17) is a very rare chromosomal disorder characterised by multiple craniofacial (microcephaly and eye, ear, and nose deformities), limb and other multiple organ abnormalities, growth and motor retardation and intellectual deficit. The syndrome is frequently lethal.
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ID_19213480
    English
    Distal 17q deletion
    Chromosome 17q deletion syndrome (deletion of the long arm of chromosome 17) is a very rare chromosomal disorder characterised by multiple craniofacial (microcephaly and eye, ear, and nose deformities), limb and other multiple organ abnormalities, growth and motor retardation and intellectual deficit. The syndrome is frequently lethal.

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      CID11:ID_19213480
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      dki-india-ID_19213480
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      Concluído
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      15 August 2026
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