Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Protein S Deficiency

Synonyms

Hereditary Thrombophilia Due To Protein S Deficiency

Definitions

An autosomal dominant disorder showing decreased levels of plasma protein S antigen or activity, associated with venous thrombosis and pulmonary embolism. PROTEIN S is a vitamin K-dependent plasma protein that inhibits blood clotting by serving as a cofactor for activated PROTEIN C (also a vitamin K-dependent protein), and the clinical manifestations of its deficiency are virtually identical to those of protein C deficiency. Treatment with heparin for acute thrombotic processes is usually followed by maintenance administration of coumarin drugs for the prevention of recurrent thrombosis. (From Harrison's Principles of Internal Medicine, 12th ed, p1511; Wintrobe's Clinical Hematology, 9th ed, p1523)

ID

http://purl.bioontology.org/ontology/MESH/D018455

altLabel

Hereditary Thrombophilia Due To Protein S Deficiency

Deficiency, Protein S

Protein S Deficiencies

Deficiencies, Protein S

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

C0242666

DC

1

definition

An autosomal dominant disorder showing decreased levels of plasma protein S antigen or activity, associated with venous thrombosis and pulmonary embolism. PROTEIN S is a vitamin K-dependent plasma protein that inhibits blood clotting by serving as a cofactor for activated PROTEIN C (also a vitamin K-dependent protein), and the clinical manifestations of its deficiency are virtually identical to those of protein C deficiency. Treatment with heparin for acute thrombotic processes is usually followed by maintenance administration of coumarin drugs for the prevention of recurrent thrombosis. (From Harrison's Principles of Internal Medicine, 12th ed, p1511; Wintrobe's Clinical Hematology, 9th ed, p1523)

DX

19950101

HN

95

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/D014813

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

http://purl.bioontology.org/ontology/MESH/D011697

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

http://purl.bioontology.org/ontology/MESH/D000361

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

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

http://purl.bioontology.org/ontology/MESH/D004406

http://purl.bioontology.org/ontology/MESH/D011693

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

http://purl.bioontology.org/ontology/MESH/D010265

http://purl.bioontology.org/ontology/MESH/D006942

http://purl.bioontology.org/ontology/MESH/D004438

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

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

http://purl.bioontology.org/ontology/MESH/D020147

http://purl.bioontology.org/ontology/MESH/D007019

Machine permutation

95

Mapped from

http://purl.bioontology.org/ontology/MESH/C567077

http://purl.bioontology.org/ontology/MESH/C567347

http://purl.bioontology.org/ontology/MESH/C567348

MDA

19940416

MMR

20130708

MN

C15.378.100.800

C15.378.925.800

C15.378.147.890

notation

D018455

prefLabel

Protein S Deficiency

TERMUI

T054987

T054988

T842345

TH

NLM (1995)

GHR (2014)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D001796

http://purl.bioontology.org/ontology/MESH/D019851

http://purl.bioontology.org/ontology/MESH/D001778

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/D68.59 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/MTHU038923 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/MTHU038923 Online Mendelian Inheritance in Man LOOM
http://purl.obolibrary.org/obo/DOID_2451 Human Disease Ontology 123 LOOM