Hereditary factor X deficiency (Q39581): Difference between revisions
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A deficiência congênita do fator X é um distúrbio hemorrágico hereditário causado por uma diminuição do antígeno ou da atividade do fator X (FX) e caracterizado por manifestações de sangramento leve a grave. | |||
| description / en | description / en | ||
Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterised by mild to severe bleeding symptoms. | |||
Revision as of 05:03, 13 August 2026
Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterised by mild to severe bleeding symptoms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B14.1 |
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| English | Hereditary factor X deficiency |
Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterised by mild to severe bleeding symptoms. |
