Hereditary deficiency of other clotting factors

Preferred Label : Hereditary deficiency of other clotting factors;

Inclusion CIM-10 : Hypoproconvertinemia; Proaccelerin deficiency; AC globulin deficiency; Deficiency of factor XII [Hageman]; Deficiency of factor I [fibrinogen]; Dysfibrinogenemia (congenital); Deficiency of factor II [prothrombin]; Deficiency of factor V [labile]; Deficiency of factor VII [stable]; Owren's disease; Deficiency of factor X [Stuart-Prower]; Deficiency of factor XIII [fibrin stabilizing]; Congenital afibrinogenemia;

Diag associé à un acte (%) : 37.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D682;

UMLS CUI

C0494242;

Automatic exact mappings (from CISMeF team)
- Congenital dysfibrinogenemia [MedDRA LLT]
- Congenital factor VII deficiency [ORDO Disease]
- Dysfibrinogenemia, congenital [OMIM Phenotype]
- Hereditary Factor V Deficiency [NCIt concept]
- Hereditary dysfibrinogenemia (disorder) [SNOMED CT concept]
- afibrinogenemia [MeSH Descriptor]
- factor v deficiency [MeSH Descriptor]
- factor vii deficiency [MeSH Descriptor]
DO Cross reference
- factor V deficiency [DO Concept]
- factor VII deficiency [DO Concept]
Orphanet concepts
- Congenital factor II deficiency [ORDO Disease]
- Congenital factor V deficiency [ORDO Disease]
- Congenital factor VII deficiency [ORDO Disease]
- Congenital factor X deficiency [ORDO Disease]
- Congenital factor XII deficiency [ORDO Disease]
- Congenital factor XIII deficiency [ORDO Disease]
- Congenital fibrinogen deficiency [ORDO Disease]
- Congenital vitamin K-dependent coagulation factors deficiency [ORDO Disease]
- East Texas bleeding disorder [ORDO Disease]
- Familial afibrinogenemia [ORDO Disease]
- Familial dysfibrinogenemia [ORDO Disease]
- Familial hypodysfibrinogenemia [ORDO Disease]
- Familial hypofibrinogenemia [ORDO Disease]
- Hereditary combined deficiency of vitamin K-dependent clotting factors [ORDO Disease]
- Severe hereditary thrombophilia due to congenital protein C deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Afibrinogenemia, congenital [OMIM Phenotype]
- Congenital afibrinogenemia (disorder) [SNOMED CT concept]
- Congenital factor V deficiency [ORDO Disease]
- Factor VII deficiency [OMIM Phenotype]
- Hereditary factor V deficiency [ICD-11 More detail]
- Hereditary factor V deficiency disease (disorder) [SNOMED CT concept]
- congenital afibrinogenemia [DO Concept]
- factor V deficiency [DO Concept]
- factor v deficiency [Blood Transfusion thesaurus concept]
- factor vii deficiency [Blood Transfusion thesaurus concept]

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