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Factor V Deficiency MeSH Descriptor Data 2021


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
Factor V Deficiency Preferred
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