factor v deficiency

Preferred Label : factor v deficiency;

MeSH definition : A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed);

MeSH synonym : disease, owren; owren's disease; owrens disease; disease, owren's; deficiency, factor v; owren disease; deficiencies, factor v; factor v deficiencies; parahemophilias; parahemophilia; labile factor deficiency; deficiencies, labile factor; deficiency, labile factor; labile factor deficiencies; owren parahemophilia; parahemophilia, owren; Factor Five Deficiency; Deficiencies, Factor Five; Factor Five Deficiencies; Deficiency, Factor 5; Deficiency, Factor Five; Factor 5 Deficiency; Deficiencies, Factor 5; Factor 5 Deficiencies;

CISMeF synonym : diseases, owren; diseases, owren's; owren diseases; owren's diseases;

MeSH annotation : a blood coag disord; DF: FACTOR V DEFIC; a blood coag disord;

Details

Origin ID

D005166;

UMLS CUI

C0015499;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Complement factor D deficiency [OMIM Phenotype]
- Complement factor h deficiency [OMIM Phenotype]
- Factor II deficiency [MedDRA Preferred Term]
- Factor III deficiency [MedDRA Preferred Term]
- Factor X deficiency [PASCAL descriptor]
- Factor X deficiency [OMIM Phenotype]
- Factor X deficiency [MedDRA Preferred Term]
- Hereditary deficiency of other clotting factors [ICD-10 Sub-category]
- Hereditary deficiency of other clotting factors [ICD-10 Sub-category (who)]
- Hereditary factor V deficiency [ICD-11 More detail]
- PROTHROMBIN TIME PROLONGED [WHO-ART Included Term]
- factor V deficiency [DO Concept]
- factor ii deficiency [TUV Concept]
- factor ii deficiency, nos [SNOMED Notion]
- factor x deficiency, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital factor V deficiency [ORDO Disease]
- Factor V Deficiency [NCIt concept]
- Factor V deficiency [MedDRA Preferred Term]
- Factor V deficiency [OMIM Phenotype]
- Factor V deficiency (disorder) [SNOMED CT concept]
- Hereditary Factor V Deficiency [NCIt concept]
- Hereditary factor V deficiency disease (disorder) [SNOMED CT concept]
- Reduced coagulation factor V activity [HPO term]
- blood clotting factor v deficiency [Disease (Nov.)]
- factor v deficiency [Blood Transfusion thesaurus concept]
- factor v deficiency, nos [SNOMED Notion]
- hereditary factor v deficiency disease [SNOMED Notion]
DO Cross reference
- factor V deficiency [DO Concept]
HPO term
- Reduced coagulation factor V activity [HPO term]
Manual NTBT mappings (CISMeF)
- Alpha granule disease [ORDO Disease]
- Rare hemorrhagic disorder due to a constitutional coagulation factors defect [ORDO Disease]
MeSH Descriptor(s) used for indexing
- factor v [MeSH Descriptor]
Record concept(s)
- factor V deficiency [MeSH concept]
Related MeSH Supplementary Concept(s)
- familial multiple coagulation factor deficiency I [MeSH Supplementary Concept]
- quebec platelet disorder [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital factor V deficiency [ORDO Disease]
- Factor V deficiency [OMIM Phenotype]
- Hereditary Factor V Deficiency [NCIt concept]
- Hereditary factor V deficiency disease (disorder) [SNOMED CT concept]
- Reduced coagulation factor V activity [HPO term]
- factor V deficiency [DO Concept]
- factor v deficiency, nos [SNOMED Notion]
- hereditary factor v deficiency disease [SNOMED Notion]

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