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Toxic epidermal necrolysis

disorder
SNOMED 768962006CUI C0014518

Overview

By MedlinePlus, National Library of Medicine

NIH: National Institute of Arthritis and Musculoskeletal and Skin Diseases Courtesy of the National Library of Medicine. Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Blister
Very frequent (80-99%)HP:0008066
Deglutition disorder
Very frequent (80-99%)HP:0002015
Erythema
Very frequent (80-99%)HP:0010783
Extreme thirst
Very frequent (80-99%)HP:0001959
Flat, discolored area of skin
Very frequent (80-99%)HP:0012733
Infection in blood stream
Very frequent (80-99%)HP:0100806
Neutropoenia
Very frequent (80-99%)HP:0001875
Nikolsky's sign
Very frequent (80-99%)HP:0100792
Thrombocytopenia
Very frequent (80-99%)HP:0001873
Tiredness
Very frequent (80-99%)HP:0012378
Weight loss
Very frequent (80-99%)HP:0001824
Coughing
Frequent (30-79%)HP:0012735
Dull burning sensation with urination
Frequent (30-79%)HP:0100518
Intestinal malabsorption
Frequent (30-79%)HP:0002024
Low number of red blood cells or hemoglobin
Frequent (30-79%)HP:0001903
Oversalivation
Frequent (30-79%)HP:0003781
respiratory infections, recurrent
Frequent (30-79%)HP:0002205
Subclinical abnormal liver function tests
Frequent (30-79%)HP:0002910
Upset stomach
Frequent (30-79%)HP:0002027
Abnormal connection between trachea and esophagus
Occasional (5-29%)HP:0002575
Abnormal myocardium morphology
Occasional (5-29%)HP:0001637
Abnormal pleura morphology
Occasional (5-29%)HP:0002103
Abnormal vagina morphology
Occasional (5-29%)HP:0000142
Acute liver failure
Occasional (5-29%)HP:0006554
Conjunctivitis
Occasional (5-29%)HP:0000509
Corneal erosion
Occasional (5-29%)HP:0200020
Eyelid turned in
Occasional (5-29%)HP:0000621
Gastrointestinal haemorrhage
Occasional (5-29%)HP:0002239
Intestinal perforation
Occasional (5-29%)HP:0031368
Laboured breathing
Occasional (5-29%)HP:0002098

Quick Facts

SNOMED CT
768962006
UMLS CUI
C0014518
Fully Specified Name
Lyell 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.