Bernard-Soulier syndrome (Q93445): Difference between revisions
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Latest revision as of 08:33, 16 August 2026
Bernard-Soulier Syndrome, also known as haemorrhagiparous thrombocytic dystrophy, is a hereditary bleeding disorder affecting the megakaryocyte/platelet lineage and characterised by bleeding tendency, giant blood platelets and low platelet counts.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_507309898 |
||
| English | Bernard-Soulier syndrome |
Bernard-Soulier Syndrome, also known as haemorrhagiparous thrombocytic dystrophy, is a hereditary bleeding disorder affecting the megakaryocyte/platelet lineage and characterised by bleeding tendency, giant blood platelets and low platelet counts. |
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CID11:ID_507309898
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dki-india-ID_507309898
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Concluído
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15 August 2026
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