Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Factor V Deficiency
Synonyms

Disease, Owren
Definitions

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)
ID

http://purl.bioontology.org/ontology/MESH/D005166
altLabel

Disease, Owren

Deficiencies, Factor Five

Owren Parahemophilia

Owrens Disease

Factor Five Deficiencies

Owren Disease

Deficiency, Factor Five

Parahemophilias

Deficiencies, Labile Factor

Labile Factor Deficiency

Factor 5 Deficiency

Deficiency, Factor V

Parahemophilia, Owren

Factor Five Deficiency

Labile Factor Deficiencies

Deficiencies, Factor 5

Deficiency, Factor 5

Disease, Owren's

Parahemophilia

Factor 5 Deficiencies

Owren's Disease

Deficiencies, Factor V

Factor V Deficiencies

Deficiency, Labile Factor
AN

a blood coag disord
AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui

C0015499
DC

1
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)
DX

19730101
HN

73(64); was see under HYPOPROTHROMBINEMIAS 1963-72
Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469
Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D000347

http://purl.bioontology.org/ontology/MESH/D005171

http://purl.bioontology.org/ontology/MESH/D014813

http://purl.bioontology.org/ontology/MESH/D020141

http://purl.bioontology.org/ontology/MESH/D014923

http://purl.bioontology.org/ontology/MESH/D004211

http://purl.bioontology.org/ontology/MESH/D020151

http://purl.bioontology.org/ontology/MESH/D020016

http://purl.bioontology.org/ontology/MESH/D013915

http://purl.bioontology.org/ontology/MESH/D014842

http://purl.bioontology.org/ontology/MESH/D005173

http://purl.bioontology.org/ontology/MESH/D014884

http://purl.bioontology.org/ontology/MESH/D005177

http://purl.bioontology.org/ontology/MESH/D005168

http://purl.bioontology.org/ontology/MESH/D013920

http://purl.bioontology.org/ontology/MESH/D001606

http://purl.bioontology.org/ontology/MESH/D007020

http://purl.bioontology.org/ontology/MESH/D055652

http://purl.bioontology.org/ontology/MESH/D022861

http://purl.bioontology.org/ontology/MESH/D005175

http://purl.bioontology.org/ontology/MESH/D016553

http://purl.bioontology.org/ontology/MESH/D020152

http://purl.bioontology.org/ontology/MESH/D006467

http://purl.bioontology.org/ontology/MESH/D002836

http://purl.bioontology.org/ontology/MESH/D010981
Machine permutation

73; was see under HYPOPROTHROMBINEMIAS 1963-72
Mapped from

http://purl.bioontology.org/ontology/MESH/C565577

http://purl.bioontology.org/ontology/MESH/C536260
MDA

19990101
MMR

20170502
MN

C15.378.463.300

C15.378.100.100.300

C16.320.099.300

C15.378.100.141.300
notation

D005166
OL

use HYPOPROTHROMBINEMIAS to search FACTOR V DEFICIENCY 1966-72
prefLabel

Factor V Deficiency
TERMUI

T000913531

T811527

T015789

T015792

T000913528

T015790

T015791

T015788

T811528

T000913530

T000913529
TH

UNK (19XX)

NLM (2018)

NLM (1964)

OMIM (2013)

NLM (1999)
tui

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D006474

http://purl.bioontology.org/ontology/MESH/D025861

http://purl.bioontology.org/ontology/MESH/D020147
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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_2216 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU023372 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/227400 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/227400 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/ICD10CM/D68.2 International Classification of Diseases, Version 10 - Clinical Modification CUI