Hereditary antithrombin III deficiency

disorder

SNOMED 439699000CUI C2586031

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.

Antithrombin III deficiency

Very frequent (80-99%)HP:0001976

Reduced antithrombin antigen

Very frequent (80-99%)HP:0040246

Blood clot in artery of lung

Frequent (30-79%)HP:0002204

Deep venous thrombosis

Frequent (30-79%)HP:0002625

Recurrent thromboembolism

Frequent (30-79%)HP:0004831

Superficial thrombophlebitis

Frequent (30-79%)HP:0002638

Blood clot in artery

Occasional (5-29%)HP:0004420

Hepatic venous thrombosis

Occasional (5-29%)HP:0030243

Mesenteric venous thrombosis

Occasional (5-29%)HP:0030248

Portal vein thrombosis

Occasional (5-29%)HP:0030242

Retinal vein occlusion

Occasional (5-29%)HP:0012636

Cerebral thrombosis

Very rare (1-4%)HP:0005305

Related Conditions

Hereditary thrombophilia(parent)

Antithrombin III deficiency(parent)

Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT: 439699000
UMLS CUI: C2586031
Fully Specified Name: Hereditary antithrombin III deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.