Primary inherited erythrocytosis (Q39677): Difference between revisions
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Doença causada por fatores herdados geneticamente levando a alterações na concentração dos glóbulos vermelhos. Esta doença é caracterizada por apresentar altas concentrações de glóbulos vermelhos no corpo levando a fluxo sanguíneo lento. A confirmação é feita pela identificação de mutações por testagem genética. | |||
| description / en | description / en | ||
A disease caused by genetically inherited factors leading to changes in the concentration of red blood cells. This disease is characterised by having a high concentration of red blood cells in the body leading to slow flow of blood. Confirmation is by identification of mutations by genetic testing. | |||
Revision as of 05:11, 13 August 2026
A disease caused by genetically inherited factors leading to changes in the concentration of red blood cells. This disease is characterised by having a high concentration of red blood cells in the body leading to slow flow of blood. Confirmation is by identification of mutations by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A80.0 |
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| English | Primary inherited erythrocytosis |
A disease caused by genetically inherited factors leading to changes in the concentration of red blood cells. This disease is characterised by having a high concentration of red blood cells in the body leading to slow flow of blood. Confirmation is by identification of mutations by genetic testing. |
