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VEXAS syndrome

disorder
SNOMED 1290093003CUI C5435753

Overview

VEXAS syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Intermittent fever
Very frequent (80-99%)HP:0001954
Macrocytic anemia
Very frequent (80-99%)HP:0001972
Chondritis of pinna
Frequent (30-79%)HP:0200047
Lung infiltrates
Frequent (30-79%)HP:0002113
Nose chondritis
Frequent (30-79%)HP:0033380
Thromboembolic events
Frequent (30-79%)HP:0001907
Arthralgias
HP:0002829
Arthritis
HP:0001369
Autoimmune antibody positivity
HP:0030057
Deep venous thrombosis
HP:0002625
Dyserythropoiesis
HP:0031688
Dysmegakaryopoiesis
HP:0031689
Elevated C-reactive protein level
HP:0011227
Elevated sedimentation rate
HP:0003565
Hypoplastic myelodysplasia
HP:0002863
Inflammation of artery
HP:0012089
Inflammatory abnormality of the skin
HP:0011123
Low platelet count
HP:0001873
Neutrophilic infiltration of the skin
HP:0031234
Night sweats
HP:0030166
Sensorineural deafness
HP:0000407
Skin plaque
HP:0200035
Tiredness
HP:0012378

Quick Facts

SNOMED CT
1290093003
UMLS CUI
C5435753
Fully Specified Name
Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
23
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.