Drug rash with eosinophilia and systemic symptoms
General Information (adopted from Orphanet):
Synonyms, Signs: |
DRESS syndrome Drug reaction eosinophilic systemic syndrome |
Number of Symptoms | 30 |
OrphanetNr: | 139402 |
OMIM Id: |
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ICD-10: |
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UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Not applicable [Orphanet] |
Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Rare urticaria
-Rare allergic disease -Rare skin disease Toxic dermatosis -Rare skin disease |
Symptom Information:
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(HPO:0000083) | Renal insufficiency | Occasional [Orphanet] | 232 / 7739 | |||
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(HPO:0001970) | Tubulointerstitial nephritis | Occasional [Orphanet] | 27 / 7739 | |||
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(HPO:0000100) | Nephrotic syndrome | Occasional [Orphanet] | 83 / 7739 | |||
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(HPO:0011037) | Decreased urine output | Occasional [Orphanet] | 47 / 7739 | |||
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(HPO:0011830) | Abnormality of oral mucosa | Occasional [Orphanet] | 47 / 7739 | |||
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(HPO:0002383) | Encephalitis | Very frequent [Orphanet] | 41 / 7739 | |||
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(HPO:0009830) | Peripheral neuropathy | Occasional [Orphanet] | 206 / 7739 | |||
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(HPO:0100646) | Thyroiditis | Very frequent [Orphanet] | 11 / 7739 | |||
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(HPO:0001396) | Cholestasis | Occasional [Orphanet] | 136 / 7739 | |||
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(HPO:0006554) | Acute hepatic failure | Occasional [Orphanet] | 20 / 7739 | |||
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(HPO:0002910) | Elevated hepatic transaminases | Frequent [Orphanet] | 158 / 7739 | |||
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(HPO:0004325) | Decreased body weight | Very frequent [Orphanet] | 492 / 7739 | |||
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(HPO:0100665) | Angioedema | Very frequent [Orphanet] | 14 / 7739 | |||
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(HPO:0000958) | Dry skin | Very frequent [Orphanet] | 152 / 7739 | |||
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(HPO:0000988) | Skin rash | Very frequent [Orphanet] | 98 / 7739 | |||
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(HPO:0010783) | Erythema | Very frequent [Orphanet] | 138 / 7739 | |||
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(HPO:0200039) | Pustule | Occasional [Orphanet] | 20 / 7739 | |||
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(HPO:0001695) | Cardiac arrest | Very frequent [Orphanet] | 87 / 7739 | |||
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(HPO:0001637) | Abnormality of the myocardium | Occasional [Orphanet] | 76 / 7739 | |||
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(HPO:0100827) | Lymphocytosis | Frequent [Orphanet] | 5 / 7739 | |||
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(HPO:0001879) | Abnormality of eosinophils | Occasional [Orphanet] | 20 / 7739 | |||
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(HPO:0001945) | Fever | Very frequent [Orphanet] | 218 / 7739 | |||
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(HPO:0002093) | Respiratory insufficiency | Occasional [Orphanet] | 410 / 7739 | |||
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(HPO:0002113) | Pulmonary infiltrates | Frequent [Orphanet] | 36 / 7739 | |||
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(HPO:0002091) | Restrictive ventilatory defect | Frequent [Orphanet] | 46 / 7739 | |||
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(HPO:0100326) | Immunologic hypersensitivity | Very frequent [Orphanet] | 28 / 7739 | |||
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(HPO:0002716) | Lymphadenopathy | Very frequent [Orphanet] | 129 / 7739 | |||
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(MedDRA:10025421) | Macule | Very frequent [Orphanet] | 55 / 7739 | |||
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([DEL]MedDRA:10011224) | Cough | Occasional [Orphanet] | 70 / 7739 | |||
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(HPO:0030350) | Erythematous papule | Very frequent [Orphanet] | 123 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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