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Factor VII Deficiency MeSH Descriptor Data 2021


MeSH Heading
Factor VII Deficiency
Tree Number(s)
C15.378.100.100.310
C15.378.100.141.310
C15.378.463.310
C16.320.099.310
Unique ID
D005168
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D005168
Scope Note
An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation.
Entry Version
FACTOR VII DEFIC
Entry Term(s)
Deficiency, Factor 7
Deficiency, Factor Seven
Deficiency, Factor VII
Factor 7 Deficiency
Hypoproconvertinemia
Public MeSH Note
85; was HYPOPROCONVERTINEMIA 1963-84
Online Note
use FACTOR VII DEFICIENCY to search HYPOPROCONVERTINEMIA 1966-84
History Note
85; was HYPOPROCONVERTINEMIA 1963-84
Date Established
1985/01/01
Date of Entry
1999/01/01
Revision Date
2017/05/02
Factor VII Deficiency Preferred
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