ADP platelet receptor P2Y12 deficiency (Q84808): Difference between revisions
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Revision as of 10:09, 15 August 2026
Congenital deficiency of the P2Y12 ADP receptor is a rare autosomal recessive disorder of platelets that gives rise to a mild bleeding syndrome marked by excessive posttraumatic and postsurgical blood loss.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_121084770 |
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| English | ADP platelet receptor P2Y12 deficiency |
Congenital deficiency of the P2Y12 ADP receptor is a rare autosomal recessive disorder of platelets that gives rise to a mild bleeding syndrome marked by excessive posttraumatic and postsurgical blood loss. |
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CID11:ID_121084770
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dki-india-ID_121084770
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Concluído
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