Hereditary thrombocytopenia (Q39631): Difference between revisions
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Doença causa por uma mutação geneticamente herdada levando à contagem diminuída de plaquetas. Essa doença é caracterizada por níveis baixos de plaquetas no sangue. Pode apresentar-se com aumento na ocorrência de equimoses ou hemorragias. A confirmação é feita pela identificação de contagem plaquetária baixa em amostra de sangue. | |||
| description / en | description / en | ||
A disease caused by a genetically inherited mutation leading to decreased platelet count. This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased platelet count in a blood sample. | |||
Revision as of 05:07, 13 August 2026
A disease caused by a genetically inherited mutation leading to decreased platelet count. This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased platelet count in a blood sample.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B64.01 |
||
| English | Hereditary thrombocytopenia |
A disease caused by a genetically inherited mutation leading to decreased platelet count. This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased platelet count in a blood sample. |
