Dengue fever

Dengue fever (DF), caused by dengue virus, is an arboviral disease characterized by an initial non-specific febrile illness that can sometimes progress to more severe forms manifesting capillary leakage and hemorrhage (dengue hemorrhagic fever, or DHF) and shock (dengue shock syndrome, or DSS).



Input patient's signs and symptoms


Narrow down the case reports



Total: 426 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
17
(38.2%)
17368695
Dengue fever mimicking acute appendicitis.
Premaratna R, Bailey MS, Ratnasena BG, de Silva HJ.
Trans R Soc Trop Med Hyg. 2007;101(7):683-5.
Petechiae Fever
Abdominal Pain Acute Disease Adult Appendicitis Dengue Fever Differential Diagnosis Females Fever Homo sapiens Male
17
(38.2%)
16283129
[Hemorrhagic dengue fever after trip to Malaysia].
Hafner C, Koellner K, Vogt T, Landthaler M, Szeimies RM.
Hautarzt. 2006;57(8):705-7.
Petechiae Fever
Adult Antibodies, Viral Dengue Virus Differential Diagnosis Germany Homo sapiens Immunoglobulin M Malaysia Male Severe Dengue Skin
17
(38.2%)
10063209
A Japanese case of dengue fever with lymphocytic vasculitis: diagnosis by polymerase chain reaction.
Ishikawa H, Okada S, Katayama I, Mazaki H, Nagatake T, Hasebe F, Igarashi A.
J Dermatol. 1999;26(1):29-32.
Purpura Fever
Adult Dengue Fever Homo sapiens Male Polymerase Chain Reaction Skin Skin Diseases, Vascular T-Lymphocyte Vasculitis
17
(38.2%)
9229755
[A case of autoimmune thrombocytopenic purpura and dengue].
Rodriguez-Angulo EM, Sosa Munoz J, Garcia-Miss MR, Farfan-Ale JA, Lorono-Pino MA.
Rev Invest Clin. 1997;49(1):47-9.
Purpura Fever
Adult Dengue Fever Homo sapiens Male
25
(37.8%)
28818105
(5561569)
Severe neutropenia revealing a rare presentation of dengue fever: a case report.
Shourick J, Dinh A, Matt M, Salomon J, Davido B.
BMC Res Notes. 2017;10(1):415.
Thrombocytopenia Fever Viral hepatitis
Adult Dengue Fever Dengue Virus Females France Homo sapiens Neutropenia Thailand Viral Nonstructural Proteins
25
(37.8%)
26506741
FATAL RHABDOMYOLYSIS IN DENGUE HEMORRHAGIC FEVER: A CASE REPORT.
Siriyakorn N, Insiripong S.
Southeast Asian J Trop Med Public Health. 2015;46 Suppl 1:149-52.
Thrombocytopenia Dehydration Hepatitis
Fatal Outcome Homo sapiens Male Renal Dialysis Rhabdomyolysis Severe Dengue Thailand
25
(37.8%)
17306619
Fulminant hepatitis in dengue haemorrhagic fever.
Ling LM, Wilder-Smith A, Leo YS.
J Clin Virol. 2007;38(3):265-8.
Thrombocytopenia Fever Fulminant hepatitis
Hepatitis, Viral, Human Homo sapiens Liver Failure, Acute Male Middle Aged Severe Dengue Transaminases
25
(37.8%)
15880238
Dengue hemorrhagic fever and acute hepatitis: a case report.
Mourao MP, Lacerda MV, Bastos Mde S, Albuquerque BC, Alecrim WD.
Braz J Infect Dis. 2004;8(6):461-4.
Epistaxis Fever Hepatitis
Acute Disease Adult Enzyme-Linked Immunosorbent Assay Hepatitis Homo sapiens Male Severe Dengue Severity of Illness Index
25
(37.8%)
11725386
Dengue fever in the Czech Republic.
Chalupa P, Kubek J, Hejlova A.
Bratisl Lek Listy. 2001;102(7):322-5.
Thrombocytopenia Fever Viral hepatitis
SLC17A5
Adult Czech Republic Dengue Fever Females Homo sapiens Male Thailand
30
(37.6%)
26563725
[Acute renal failure after dengue virus infection: A pediatric case report].
Nicolon C, Broustal E.
Arch Pediatr. 2016;23(1):53-5.
Thrombocytopenia Hemolytic anemia Fever Shock
Child Dengue Fever Guadeloupe Homo sapiens Male Red Blood Cell Transfusion Remission, Spontaneous
        

Phenotype(s) retrieved from Orphanet

    Total: 22

HPO ID Term Frequency
HP:0001945 Fever Very frequent (99-80%)
HP:0002315 Headache Very frequent (99-80%)
HP:0000988 Skin rash Frequent (79-30%)
HP:0000989 Pruritus Frequent (79-30%)
HP:0002027 Abdominal pain Frequent (79-30%)
HP:0002829 Arthralgia Frequent (79-30%)
HP:0000225 Gingival bleeding Occasional (29-5%)
HP:0000421 Epistaxis Occasional (29-5%)
HP:0000967 Petechiae Occasional (29-5%)
HP:0000978 Bruising susceptibility Occasional (29-5%)
HP:0001254 Lethargy Occasional (29-5%)
HP:0001342 Cerebral hemorrhage Occasional (29-5%)
HP:0001541 Ascites Occasional (29-5%)
HP:0001873 Thrombocytopenia Occasional (29-5%)
HP:0001882 Leukopenia Occasional (29-5%)
HP:0002014 Diarrhea Occasional (29-5%)
HP:0002017 Nausea and vomiting Occasional (29-5%)
HP:0002239 Gastrointestinal hemorrhage Occasional (29-5%)
HP:0002240 Hepatomegaly Occasional (29-5%)
HP:0002615 Hypotension Occasional (29-5%)
HP:0003075 Hypoproteinemia Occasional (29-5%)
HP:0006543 Cardiorespiratory arrest Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 125

HPO ID Term # of case reports
HP:0001945 Fever 82
HP:0031273 Shock 27
HP:0001873 Thrombocytopenia 19
HP:0001298 Encephalopathy 11
HP:0003201 Rhabdomyolysis 11
HP:0012486 Myelitis 9
HP:0003326 Myalgia 7
HP:0001735 Acute pancreatitis 6
HP:0002315 Headache 6
HP:0002829 Arthralgia 6
HP:0012223 Splenic rupture 6
HP:0001082 Cholecystitis 5
HP:0001919 Acute kidney injury 5
HP:0012115 Hepatitis 5
HP:0000505 Visual impairment 4
HP:0001882 Leukopenia 4
HP:0002027 Abdominal pain 4
HP:0002170 Intracranial hemorrhage 4
HP:0012156 Hemophagocytosis 4
HP:0100614 Myositis 4
HP:0000572 Visual loss 3
HP:0000618 Blindness 3
HP:0002014 Diarrhea 3
HP:0002615 Hypotension 3
HP:0002721 Immunodeficiency 3
HP:0012819 Myocarditis 3
HP:0030150 Plasmacytosis 3
HP:0100758 Gangrene 3
HP:0000020 Urinary incontinence 2
HP:0000099 Glomerulonephritis 2
HP:0000112 Nephropathy 2
HP:0000123 Nephritis 2
HP:0000603 Central scotoma 2
HP:0000952 Jaundice 2
HP:0001138 Optic neuropathy 2
HP:0001250 Seizures 2
HP:0001251 Ataxia 2
HP:0001698 Pericardial effusion 2
HP:0001876 Pancytopenia 2
HP:0002013 Vomiting 2
HP:0002181 Cerebral edema 2
HP:0002480 Hepatic encephalopathy 2
HP:0002902 Hyponatremia 2
HP:0003470 Paralysis 2
HP:0100282 Acute colitis 2
HP:0100646 Thyroiditis 2
HP:0100653 Optic neuritis 2
HP:0000016 Urinary retention 1
HP:0000421 Epistaxis 1
HP:0000488 Retinopathy 1
HP:0000501 Glaucoma 1
HP:0000508 Ptosis 1
HP:0000509 Conjunctivitis 1
HP:0000544 External ophthalmoplegia 1
HP:0000575 Scotoma 1
HP:0000704 Periodontitis 1
HP:0000829 Hypoparathyroidism 1
HP:0000836 Hyperthyroidism 1
HP:0000873 Diabetes insipidus 1
HP:0000967 Petechiae 1
HP:0000969 Edema 1
HP:0000979 Purpura 1
HP:0000988 Skin rash 1
HP:0001085 Papilledema 1
HP:0001260 Dysarthria 1
HP:0001271 Polyneuropathy 1
HP:0001281 Tetany 1
HP:0001287 Meningitis 1
HP:0001300 Parkinsonism 1
HP:0001336 Myoclonus 1
HP:0001369 Arthritis 1
HP:0001399 Hepatic failure 1
HP:0001541 Ascites 1
HP:0001649 Tachycardia 1
HP:0001662 Bradycardia 1
HP:0001678 Atrioventricular block 1
HP:0001701 Pericarditis 1
HP:0001875 Neutropenia 1
HP:0001888 Lymphopenia 1
HP:0001903 Anemia 1
HP:0001944 Dehydration 1
HP:0002018 Nausea 1
HP:0002078 Truncal ataxia 1
HP:0002090 Pneumonia 1
HP:0002140 Ischemic stroke 1
HP:0002148 Hypophosphatemia 1
HP:0002202 Pleural effusion 1
HP:0002248 Hematemesis 1
HP:0002583 Colitis 1
HP:0002586 Peritonitis 1
HP:0002653 Bone pain 1
HP:0002835 Aspiration 1
HP:0002901 Hypocalcemia 1
HP:0005268 Spontaneous abortion 1
HP:0005305 Cerebral venous thrombosis 1
HP:0005521 Disseminated intravascular coagulation 1
HP:0006562 Viral hepatitis 1
HP:0006597 Diaphragmatic paralysis 1
HP:0008682 Acute tubular necrosis 1
HP:0009830 Peripheral neuropathy 1
HP:0010543 Opsoclonus 1
HP:0011458 Abdominal symptom 1
HP:0011506 Choroidal neovascularization 1
HP:0011709 Atrioventricular dissociation 1
HP:0011854 Hemoperitoneum 1
HP:0011921 Exudative pleural effusion 1
HP:0011974 Myelofibrosis 1
HP:0012109 Angle closure glaucoma 1
HP:0012378 Fatigue 1
HP:0012597 Heavy proteinuria 1
HP:0012636 Retinal vein occlusion 1
HP:0020071 Viremia 1
HP:0025337 Red eye 1
HP:0025342 Central retinal artery occlusion 1
HP:0025615 Abscess 1
HP:0031364 Ecchymosis 1
HP:0031864 Bacteremia 1
HP:0031931 Ocular flutter 1
HP:0040223 Pulmonary hemorrhage 1
HP:0045073 Serositis 1
HP:0100279 Ulcerative colitis 1
HP:0100519 Anuria 1
HP:0100532 Scleritis 1
HP:0100806 Sepsis 1
HP:0100827 Lymphocytosis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID