19p13.12 deletion (Q65356): Difference between revisions
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A síndrome de microdeleção 19p13.12 é uma anomalia cromossômica associada a atraso de desenvolvimento moderado a grave, atraso de linguagem, perda auditiva neurossensorial e/ou condutiva bilateral e dismorfismo facial. | |||||||||||||||
| description / en | description / en | ||||||||||||||
19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1258292853 / rank | |||||||||||||||
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CID11:ID_1258292853 | |||||||||||||||
| Property / CURIE: CID11:ID_1258292853 / rank | |||||||||||||||
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dki-india-ID_1258292853 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1258292853 / 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
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 13:04, 14 August 2026
19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1258292853 |
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| English | 19p13.12 deletion |
19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism. |
Statements
CID11:ID_1258292853
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dki-india-ID_1258292853
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Concluído
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13 August 2026
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