Hereditary hypofibrinogenaemia

Preferred Label : Hereditary hypofibrinogenaemia;

ICD-11 definition : Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration.;

ICD-11 inclusion : congenital hypofibrinogenaemia;

Details

Origin ID

559585471;

Automatic exact mappings (from CISMeF team)
- Hereditary factor I deficiency disease (disorder) [SNOMED CT concept]
- hereditary factor i deficiency disease, nos [SNOMED Notion]

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