Hereditary thrombophilia due to congenital protein S deficiency (Q52594): Difference between revisions
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Deficiência congênita de proteína S é um transtorno hereditário da coagulação caracterizado por sintomas de trombose venosa recorrente devido à redução da síntese e/ou dos níveis de atividade da proteina S. | |||
| description / en | description / en | ||
Congenital protein S deficiency is an inherited coagulation disorder characterised by recurrent venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein S. | |||
Revision as of 23:53, 13 August 2026
Congenital protein S deficiency is an inherited coagulation disorder characterised by recurrent venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein S.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1305244529 |
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| English | Hereditary thrombophilia due to congenital protein S deficiency |
Congenital protein S deficiency is an inherited coagulation disorder characterised by recurrent venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein S. |
