Hereditary factor X deficiency

ICD-11 code : 3B14.1;

Preferred Label : Hereditary factor X deficiency;

ICD-11 definition : Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms.;

ICD-11 synonym : Stuart-Prower factor deficiency; Congenital Stuart factor deficiency;

ICD-11 inclusion : congenital factor x deficiency; Stuart deficiency disease; Stuart-Prower disease; Stuart Prower deficiency; Deficiency of factor X;

Détails

Origin ID

1886781445;

Automatic exact mappings (from CISMeF team)
- Congenital factor X deficiency [ORDO Disease]
- Factor X deficiency [OMIM Phenotype]
- Factor X deficiency (disorder) [SNOMED CT concept]
- Hereditary Factor X Deficiency [NCIt concept]
- Hereditary factor X deficiency disease (disorder) [SNOMED CT concept]
- factor x deficiency [MeSH Descriptor]
ICD-10 Mapping
- Hereditary deficiency of other clotting factors [ICD-10 Sub-category]

Position du mot-clé dans l'(les) arborescence(s) :

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