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Cogan's syndrome

disorder
SNOMED 405810005CUI C0271270

Overview

Cogan's 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.

Corneal inflammation
Very frequent (80-99%)HP:0000491
Decreased visual acuity
Very frequent (80-99%)HP:0007663
Dizziness
Very frequent (80-99%)HP:0002321
Interictal vestibular dysfunction
Very frequent (80-99%)HP:0001751
Photophobia
Very frequent (80-99%)HP:0000613
Ringing in ears
Very frequent (80-99%)HP:0000360
Elevated sedimentation rate
Frequent (30-79%)HP:0003565
Increased platelet count
Frequent (30-79%)HP:0001894
Increased total leukocyte count
Frequent (30-79%)HP:0001974
Inflammatory abnormality of the eye
Frequent (30-79%)HP:0100533
Low number of red blood cells or haemoglobin
Frequent (30-79%)HP:0001903
Sensorineural deafness
Frequent (30-79%)HP:0000407
Aortic valve regurgitation
Occasional (5-29%)HP:0001659
Blindness
Occasional (5-29%)HP:0000618
Episcleritis
Occasional (5-29%)HP:0100534
Inflammation of blood vessel
Occasional (5-29%)HP:0002633
Large vessel vasculitis
Occasional (5-29%)HP:0005310
Pink eye
Occasional (5-29%)HP:0000509
Scleritis
Occasional (5-29%)HP:0100532
Uveitis
Occasional (5-29%)HP:0000554

Quick Facts

SNOMED CT
405810005
UMLS CUI
C0271270
Fully Specified Name
Cogan's syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
20
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.