Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
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

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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http://purl.obolibrary.org/obo/DOID_2216 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_2216 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU023372 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/MONDO_0020586 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0020586 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/227400 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/227400 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C131738 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/ICD10CM/D68.2 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI