Dursun syndrome (Q107334): Difference between revisions
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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 |
||
| 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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