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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   drug rash with eosinophilia and systemic symptoms
  

Disease ID 1376
Disease drug rash with eosinophilia and systemic symptoms
Definition
Severe drug eruption characterized by high fever, erythematous rash and inflammation of internal organ(s).
Synonym
anticonvulsant hypersensitivity syndrome
dress syndrome
dress syndromes
drug hypersensitivity syndrome
drug hypersensitivity syndrome [disease/finding]
drug hypersensitivity syndromes
drug reaction with eosinophilia and systemic symptoms
drug reaction with eosinophilia and systemic symptoms (disorder)
drug reaction with eosinophilia and systemic symptoms syndrome
drug-induced hypersensitivity syndrome
hypersensitivity syndrome, drug
hypersensitivity syndromes, drug
syndrome, drug hypersensitivity
syndromes, drug hypersensitivity
Orphanet
UMLS
C3541994
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:27)
C0027059  |  myocarditis  |  3
C0019158  |  hepatitis  |  3
C0027707  |  interstitial nephritis  |  3
C0027697  |  nephritis  |  3
C0011854  |  type 1 diabetes  |  3
C0011847  |  diabetes  |  2
C0019360  |  herpes zoster  |  2
C0019360  |  zoster  |  2
C0035222  |  acute respiratory distress syndrome  |  2
C1704437  |  respiratory distress syndrome  |  2
C0024291  |  hemophagocytic lymphohistiocytosis  |  2
C0011603  |  dermatitis  |  1
C0021141  |  syndrome of inappropriate secretion of antidiuretic hormone  |  1
C0009319  |  colitis  |  1
C0015230  |  rash  |  1
C0442874  |  neuropathy  |  1
C0042166  |  intermediate uveitis  |  1
C0038220  |  status epilepticus  |  1
C0011854  |  type 1 diabetes mellitus  |  1
C0041326  |  pleural tuberculosis  |  1
C0032285  |  pneumonitis  |  1
C0241910  |  autoimmune hepatitis  |  1
C0041296  |  tuberculosis  |  1
C0030305  |  pancreatitis  |  1
C0038463  |  strongyloides infection  |  1
C0042164  |  uveitis  |  1
C0031117  |  peripheral neuropathy  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1376
Disease drug rash with eosinophilia and systemic symptoms
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:28)
HP:0012733  |  Macule
HP:0002094  |  Dyspnea
HP:0001824  |  Weight loss
HP:0002383  |  Encephalitis
HP:0001970  |  Tubulointerstitial nephritis
HP:0006554  |  Acute hepatic failure
HP:0010783  |  Erythema
HP:0000083  |  Renal insufficiency
HP:0002716  |  Lymphadenopathy
HP:0100646  |  Thyroiditis
HP:0100326  |  Immunologic hypersensitivity
HP:0009830  |  Peripheral neuropathy
HP:0002113  |  Pulmonary infiltrates
HP:0100827  |  Lymphocytosis
HP:0030249  |  Enanthema
HP:0001019  |  Erythroderma
HP:0001945  |  Fever
HP:0012819  |  Myocarditis
HP:0006515  |  Interstitial pneumonitis
HP:0012735  |  Cough
HP:0000988  |  Skin rash
HP:0002910  |  Elevated hepatic transaminases
HP:0001695  |  Cardiac arrest
HP:0000100  |  Nephrotic syndrome
HP:0012115  |  Hepatitis
HP:0100665  |  Angioedema
HP:0200039  |  Pustule
HP:0001880  |  Eosinophilia
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:26)
HP:0001880  |  Eosinophilia  |  31
HP:0000123  |  Nephritis  |  3
HP:0012115  |  Liver inflammation  |  3
HP:0012819  |  Myocarditis  |  3
HP:0001970  |  Interstitial nephritis  |  3
HP:0002098  |  Respiratory distress  |  2
HP:0000969  |  Dropsy  |  2
HP:0000952  |  Yellow skin  |  1
HP:0012124  |  Intermediate uveitis  |  1
HP:0000554  |  Uveitis  |  1
HP:0001596  |  Hair loss  |  1
HP:0200119  |  Acute liver inflammation  |  1
HP:0009830  |  Peripheral neuritis  |  1
HP:0200042  |  Skin ulcer  |  1
HP:0006554  |  Acute hepatic failure  |  1
HP:0004387  |  Enterocolitis  |  1
HP:0008940  |  Generalized lymphadenopathy  |  1
HP:0001259  |  Coma  |  1
HP:0002583  |  Colitis  |  1
HP:0001289  |  Confusion  |  1
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0005318  |  Cerebral vasculitis  |  1
HP:0001399  |  Liver failure  |  1
HP:0001733  |  Pancreatic inflammation  |  1
HP:0100806  |  Sepsis  |  1
HP:0002133  |  Status epilepticus  |  1
Disease ID 1376
Disease drug rash with eosinophilia and systemic symptoms
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0014457  |  eosinophilia  |  16
C0011854  |  type 1 diabetes mellitus  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:6)
HP ID HP Name MP ID MP Name Annotation
HP:0006554Acute hepatic failureMP:0002628hepatic steatosisan accumulation of fat deposits in the liver
HP:0002910Elevated hepatic transaminasesMP:0002628hepatic steatosisan accumulation of fat deposits in the liver
HP:0000083Renal insufficiencyMP:0003335exocrine pancreatic insufficiencyinadequate synthesis and/or secretion of digestive enzymes by the exocrine portion of the pancreas, usually due to loss of acinar tissue from idiopathic atrophy or acute or chronic inflammation, causing maldigestion and malabsorption of nutrients
HP:0001970Tubulointerstitial nephritisMP:0011405tubulointerstitial nephritisdiffuse or local inflammation and edema of the interstitial tissue of the kidney, including the renal tubules; usually secondary to drug sensitization, systemic infection, graft rejection, or autoimmune disease
HP:0100326Immunologic hypersensitivityMP:0005617increased susceptibility to type IV hypersensitivity reactiongreater likelihood of developing an antigen-elicited cellular immune reaction that results in tissue damage, but does not require Ab participation; the response is seen at the area of contact
HP:0001824Weight lossMP:0005114premature hair lossrelease of fur at an earlier than expected time
Mapped by homologous gene(Total Items:25)
HP ID HP Name MP ID MP Name Annotation
HP:0012735CoughMP:0014185cerebellum atrophyacquired diminution of the size of the cerebellum associated with wasting as from death and reabsorption of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal
HP:0001945FeverMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0006554Acute hepatic failureMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0010783ErythemaMP:0013781abnormal mammary gland luminal epithelium morphologyany structural anomaly of the inner cell layer of the mammary epithelium bilayer that lines the luminal surface of mammary gland ducts and alveoli; luminal cells have only limited contact with the underlying basement membrane and surrounding connective ti
HP:0009830Peripheral neuropathyMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0006515Interstitial pneumonitisMP:0013501increased fibroblast apoptosisincrease in the timing or the number of fibroblast cells undergoing programmed cell death
HP:0002113Pulmonary infiltratesMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0001880EosinophiliaMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0002094DyspneaMP:0014185cerebellum atrophyacquired diminution of the size of the cerebellum associated with wasting as from death and reabsorption of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal
HP:0001019ErythrodermaMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0100646ThyroiditisMP:0014171increased fatty acid oxidationincreased rate or incidence of the process of removal of one or more electrons from a fatty acid, with or without the concomitant removal of a proton or protons, by reaction with an electron-accepting substance, by addition of oxygen or by removal of hydr
HP:0100827LymphocytosisMP:0011087neonatal lethality, complete penetrancedeath of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)
HP:0001695Cardiac arrestMP:0013578abnormal stomach glandular region morphologyany structural anomaly of the distinct glandular stomach area which in rodents is demarcated from the non-glandular forestomach by the limiting ridge (margo plicatus); the glandular stomach is connected to the small intestine (duodenum); the wall of the g
HP:0100665AngioedemaMP:0011087neonatal lethality, complete penetrancedeath of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)
HP:0001824Weight lossMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0002383EncephalitisMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0002910Elevated hepatic transaminasesMP:0020234decreased basal metabolismdecrease in heat production of an organism at the lowest level of cell chemistry in an inactive, awake, and fasting state
HP:0000083Renal insufficiencyMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0100326Immunologic hypersensitivityMP:0013367parotid gland inflammationlocal accumulation of fluid, plasma proteins, and leukocytes in either of the largest of the major salivary glands situated below and in front of each ear
HP:0001970Tubulointerstitial nephritisMP:0013405increased circulating lactate levelgreater amount of lactate in the blood which is produced from pyruvate by lactate dehydrogenase
HP:0200039PustuleMP:0013745abnormal eyelid margin morphologyany structural anomaly of the confluence of the mucosal surface of the conjunctiva, the edge of the orbicularis, and the cutaneous epithelium
HP:0000100Nephrotic syndromeMP:0020216decreased circulating complement protein levelless than normal levels of the serum proteins that act sequentially to allow for the direct killing of microbes, the disposal of immune complexes, and the regulation of other immune processes
HP:0002716LymphadenopathyMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0012115HepatitisMP:0013716hypolactationpartial failure, or reduced ability to produce or secrete milk from the mammary gland
HP:0000988Skin rashMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
Disease ID 1376
Disease drug rash with eosinophilia and systemic symptoms
Case(Waiting for update.)