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Antiphospholipid syndrome

disorder
SNOMED 26843008CUI C0085278

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Intrauterine growth retardation, IUGR
Very frequent (80-99%)HP:0001511
Anti-B2GPI positivity
Frequent (30-79%)HP:0032376
Anti-beta-2-Glycoprotein I IgG antibody positivity
Frequent (30-79%)HP:0034156
Anti-beta-2-Glycoprotein I IgM antibody positivity
Frequent (30-79%)HP:0034157
Anticardiolipin IgG antibody positivity
Frequent (30-79%)HP:0020136
Anticardiolipin IgM antibody positivity
Frequent (30-79%)HP:0020137
Antiphospholipid antibodies
Frequent (30-79%)HP:0003613
Blood clot in artery
Frequent (30-79%)HP:0004420
Blood clot in vein
Frequent (30-79%)HP:0004936
Female infertility
Frequent (30-79%)HP:0008222
High blood pressure
Frequent (30-79%)HP:0000822
Hypercoagulability
Frequent (30-79%)HP:0100724
Ischemic stroke
Frequent (30-79%)HP:0002140
Livedo racemosa
Frequent (30-79%)HP:0033260
Livedo reticularis
Frequent (30-79%)HP:0033505
Lupus anticoagulant
Frequent (30-79%)HP:0025343
Pain
Frequent (30-79%)HP:0012531
Premature birth
Frequent (30-79%)HP:0001622
Tiredness
Frequent (30-79%)HP:0012378
Transient ischemic attacks
Frequent (30-79%)HP:0002326
Anti-annexin-V antibody positivity
Occasional (5-29%)HP:0034101
Anti-phosphatidyl choline antibody positivity
Occasional (5-29%)HP:0034097
Anti-phosphatidyl ethanolamine antibody positivity
Occasional (5-29%)HP:0034084
Anti-phosphatidyl glycerol antibody positivity
Occasional (5-29%)HP:0034098
Anti-phosphatidyl inositol antibody positivity
Occasional (5-29%)HP:0034099
Anti-phosphatidyl serine antibody positivity
Occasional (5-29%)HP:0034100
Aortic stenosis
Occasional (5-29%)HP:0001650
Aortic valve regurgitation
Occasional (5-29%)HP:0001659
Death of body tissue due to lack of blood flow or infection
Occasional (5-29%)HP:0100758
Disease of the heart muscle
Occasional (5-29%)HP:0001638

Related Conditions

Primary antiphospholipid syndrome(child)
Secondary antiphospholipid syndrome(child)
Lupus anticoagulant disorder(child)
Asherson's syndrome(child)
Neonatal antiphospholipid syndrome(child)
Autoimmune disease(parent)
Acquired thrombophilia(parent)

Quick Facts

SNOMED CT
26843008
UMLS CUI
C0085278
Fully Specified Name
Antiphospholipid syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.