Hereditary afibrinogenaemia (Q57270): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Afibrinogenemia familiar é um transtorno da coagulação caracterizado por sintomas hemorrágicos devido à ausência completa do fibrinogênio na circulação. | |||
| description / en | description / en | ||
Familial afibrinogenaemia is a coagulation disorder characterised by bleeding symptoms due to a complete absence of circulating fibrinogen. | |||
Revision as of 04:55, 14 August 2026
Familial afibrinogenaemia is a coagulation disorder characterised by bleeding symptoms due to a complete absence of circulating fibrinogen.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_608641873 |
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| English | Hereditary afibrinogenaemia |
Familial afibrinogenaemia is a coagulation disorder characterised by bleeding symptoms due to a complete absence of circulating fibrinogen. |
