4q21 deletion (Q101696): Difference between revisions
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A síndrome de microdeleção 4q21 é uma anomalia cromossômica associada a dismorfismo facial, restrição progressiva do crescimento, déficit intelectual grave e fala ausente ou gravemente atrasada. | |||||||||||||||
| description / en | description / en | ||||||||||||||
The 4q21 microdeletion syndrome is a chromosomal anomaly associated with facial dysmorphism, progressive growth restriction, severe intellectual deficit and absent or severely delayed speech. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1946764779 / rank | |||||||||||||||
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CID11:ID_1946764779 | |||||||||||||||
| Property / CURIE: CID11:ID_1946764779 / rank | |||||||||||||||
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dki-india-ID_1946764779 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1946764779 / 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 18:32, 16 August 2026
The 4q21 microdeletion syndrome is a chromosomal anomaly associated with facial dysmorphism, progressive growth restriction, severe intellectual deficit and absent or severely delayed speech.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1946764779 |
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| English | 4q21 deletion |
The 4q21 microdeletion syndrome is a chromosomal anomaly associated with facial dysmorphism, progressive growth restriction, severe intellectual deficit and absent or severely delayed speech. |
Statements
CID11:ID_1946764779
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dki-india-ID_1946764779
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Concluído
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15 August 2026
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