Hereditary factor X deficiency (Q39581)
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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 |
||
| 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. |
Statements
CID11:3B14.1
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dki-india-3B14.1
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Concluído
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13 August 2026
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