Inherited qualitative platelet defects (Q39614): Difference between revisions
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13 August 2026
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| Property / Linked ICD 10: D69.1 / rank | |||||||||||||||
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Latest revision as of 05:05, 13 August 2026
A disease caused by genetically inherited mutations leading to abnormalities in platelets. This disease is characterised by abnormal platelet formation or function. Confirmation is by identification of mutations by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B62.0 |
||
| English | Inherited qualitative platelet defects |
A disease caused by genetically inherited mutations leading to abnormalities in platelets. This disease is characterised by abnormal platelet formation or function. Confirmation is by identification of mutations by genetic testing. |
Statements
CID11:3B62.0
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dki-india-3B62.0
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Concluído
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13 August 2026
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