MeSH Browser

MeSH Heading: Factor V Deficiency
Tree Number(s): C15.378.100.100.300; C15.378.100.141.300; C15.378.463.300; C16.320.099.300
Unique ID: D005166
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D005166
Annotation: a blood coag disord
Scope Note: 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)
Entry Version: FACTOR V DEFIC
Entry Term(s): Deficiency, Factor 5; Deficiency, Factor Five; Deficiency, Factor V; Factor 5 Deficiency; Factor Five Deficiency; Labile Factor Deficiency; Owren Disease; Owren Parahemophilia; Owren's Disease; Parahemophilia
Public MeSH Note: 73; was see under HYPOPROTHROMBINEMIAS 1963-72
Online Note: use HYPOPROTHROMBINEMIAS to search FACTOR V DEFICIENCY 1966-72
History Note: 73(64); was see under HYPOPROTHROMBINEMIAS 1963-72
Date Established: 1973/01/01
Date of Entry: 1999/01/01
Revision Date: 2017/05/02

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
  - Blood Coagulation Disorders [C15.378.100]
    - Blood Coagulation Disorders, Inherited [C15.378.100.100]

Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
  - Blood Coagulation Disorders [C15.378.100]
    - Coagulation Protein Disorders [C15.378.100.141]

Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
  - Hemorrhagic Disorders [C15.378.463]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Blood Coagulation Disorders, Inherited [C16.320.099]

Factor V Deficiency Preferred

Concept UI: M0008143
Scope Note: 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)
Terms: Factor V Deficiency Preferred Term
Term UI T015789
Date01/01/1999
LexicalTag NON
ThesaurusID; Factor Five Deficiency
Term UI T000913529
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Deficiency, Factor 5
Term UI T000913530
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Deficiency, Factor Five
Term UI T000913531
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Deficiency, Factor V
Term UI T015788
Date01/01/1986
LexicalTag NON
ThesaurusID UNK (19XX); Owren's Disease
Term UI T015790
Date03/13/1998
LexicalTag EPO
ThesaurusID NLM (1999); Owren Disease
Term UI T015791
Date03/13/1998
LexicalTag EPO
ThesaurusID NLM (1999); Parahemophilia
Term UI T015792
Date03/13/1998
LexicalTag NON
ThesaurusID; Labile Factor Deficiency
Term UI T811527
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Factor 5 Deficiency
Term UI T000913528
Date01/04/2017
LexicalTag NON
ThesaurusID NLM (2018); Owren Parahemophilia
Term UI T811528
Date11/15/2011
LexicalTag EPO
ThesaurusID OMIM (2013)

Factor V Deficiency MeSH Descriptor Data 2024