Dursun syndrome (Q107334): Difference between revisions
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A síndrome de Dursun é um transtorno genético caracterizado por hipertensão arterial pulmonar familiar, anormalidades cardíacas, incluindo defeito do septo atrial, leucopenia incluindo neutropenia intermitente, linfopenia, monocitose e anemia. | |||||||||||||||
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Dursun syndrome is a genetic disorder characterised by familial pulmonary arterial hypertension, cardiac abnormalities including atrial septal defect, leukopenia including intermittent neutropaenia, lymphopenia, monocytosis, and anaemia. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/232201917 / rank | |||||||||||||||
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CID11:ID_232201917 | |||||||||||||||
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dki-india-ID_232201917 | |||||||||||||||
| Property / Canary Token: dki-india-ID_232201917 / rank | |||||||||||||||
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Concluído | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
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Latest revision as of 14:19, 17 August 2026
Dursun syndrome is a genetic disorder characterised by familial pulmonary arterial hypertension, cardiac abnormalities including atrial septal defect, leukopenia including intermittent neutropaenia, lymphopenia, monocytosis, and anaemia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_232201917 |
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| English | Dursun syndrome |
Dursun syndrome is a genetic disorder characterised by familial pulmonary arterial hypertension, cardiac abnormalities including atrial septal defect, leukopenia including intermittent neutropaenia, lymphopenia, monocytosis, and anaemia. |
Statements
CID11:ID_232201917
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dki-india-ID_232201917
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Concluído
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16 August 2026
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