Hereditary dysfibrinogenaemia (Q59846): 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 | ||
Disfibrinogenemia familiar é um transtorno da coagulação caracterizado por uma tendência a hemorragia devido a uma anomalia funcional do fibrinogênio circulante. | |||
| description / en | description / en | ||
Familial dysfibrinogenaemia is a coagulation disorder characterised by a bleeding tendency due to a functional anomaly of circulating fibrinogen. | |||
Revision as of 07:21, 14 August 2026
Familial dysfibrinogenaemia is a coagulation disorder characterised by a bleeding tendency due to a functional anomaly of circulating fibrinogen.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_815934276 |
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| English | Hereditary dysfibrinogenaemia |
Familial dysfibrinogenaemia is a coagulation disorder characterised by a bleeding tendency due to a functional anomaly of circulating fibrinogen. |
