Fever

Symptom Information:

Symptom ID: HPO:0001945
Synonyms:
Hyperthermia [HPO:0001945]
Pyrexia [HPO:0001945]
Fever (finding) [Orphanet:54140]
Fever symptoms (finding) [Orphanet:54140]
fever [HPO:0001945]
Fever [Orphanet:54140]
Hyperthermia [OMIM:Hyperthermia]
Fever/chilling [Orphanet:54140]
Body temperature increased [Orphanet:54140]
Pyrexia [Orphanet:54140]
Body temperature increased [MedDRA:10005911]
Temperature elevation [MedDRA:10005911]
Pyrexia [MedDRA:10037660]
Chills &
fever [MedDRA:10037660]
Chills and fever [MedDRA:10037660]
Drug fever [MedDRA:10037660]
Febrile reaction [MedDRA:10037660]
Fever [MedDRA:10037660]
Fever chills [MedDRA:10037660]
Fever of unknown origin [MedDRA:10037660]
Heat production increased [MedDRA:10037660]
Heat retention [MedDRA:10037660]
High temperature [MedDRA:10037660]
Intermittent pyrexia [MedDRA:10037660]
Periodic fever [MedDRA:10037660]
PUO [MedDRA:10037660]
Pyrexia abnormal [MedDRA:10037660]
Pyrexia drug [MedDRA:10037660]
Pyrexia NOS [MedDRA:10037660]
Pyrexia of unknown origin [MedDRA:10037660]
Pyrexia of unknown origin (excl puerperal) [MedDRA:10037660]
Pyrexial [MedDRA:10037660]
Reaction febrile [MedDRA:10037660]
Slight fever [MedDRA:10037660]
Spiking temperature [MedDRA:10037660]
Slight temperature [MedDRA:10037660]
Intermittent fever [MedDRA:10037660]
Cotton fever [MedDRA:10037660]
Febricula [MedDRA:10037660]
Fluctuating fever [MedDRA:10037660]
Chronic fever [MedDRA:10037660]
Acute febrile illness [MedDRA:10037660]
Feverish [MedDRA:10037660]
Chills [MedDRA:10008531]
Chill [Orphanet:54140]
Chill (finding) [Orphanet:54140]
Chills [Orphanet:54140]
Shivering [Orphanet:54140]
Hyperthermia [MedDRA:10020843]
Quality:
Cross references:
Orphanet:54140 "Fever/chilling" [Orphanet:54140]
OMIM: "Hyperthermia" [OMIM:Hyperthermia]
UMLS:C0424755 "fever" [HPO:0001945]
UMLS:C0424755 "Fever symptoms (finding)" [Orphanet:54140]
UMLS:C0015967 "Fever" [Orphanet:54140]
UMLS:C0085593 "Chills" [Orphanet:54140]
UMLS:C0036973 "Shivering" [Orphanet:54140]
Is a (Direct Parents):
HPO         Abnormality of temperature regulation
MedDRA Febrile disorders
MedDRA Heat injuries (excl thermal burns)
Orphanet Health status anomalies
MedDRA Physical examination procedures and organ system status
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of temperature regulation(HPO:0004370)
             Fever(HPO:0001945)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    Body temperature conditions(MedDRA:10005908)
       Febrile disorders(MedDRA:10016286)
          Fever(HPO:0001945)
Injury, poisoning and procedural complications(MedDRA:10022117)
    Injuries by physical agents(MedDRA:10022119)
       Heat injuries (excl thermal burns)(MedDRA:10019338)
          Fever(HPO:0001945)
Investigations(MedDRA:10022891)
    Physical examination and organ system status topics(MedDRA:10071940)
       Physical examination procedures and organ system status(MedDRA:10071941)
          Fever(HPO:0001945)
Database Frequency: 218 / 7739
Resource:

All diseases associated with this symptom:

3-hydroxy-3-methylglutaric aciduria (Orphanet:20)
AICARDI-GOUTIERES SYNDROME 1 (OMIM:225750)
ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS (OMIM:108050)
AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS (OMIM:616050)
Acute interstitial pneumonia (Orphanet:79126)
Adult Still's disease (Orphanet:829)
Adult heart tumor (Orphanet:874)
Allergic bronchopulmonary aspergillosis (Orphanet:1164)
Alpha heavy-chain disease (Orphanet:100025)
Alveolar echinococcosis (Orphanet:284)
Anisakiasis (Orphanet:1070)
Anti-glomerular basement membrane disease (Orphanet:375)
Antisynthetase syndrome (Orphanet:81)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Atypical hemolytic uremic syndrome (Orphanet:2134)
Autoimmune hemolytic anemia (Orphanet:98375)
Autoimmune hemolytic anemia, warm type (Orphanet:90033)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
Babesiosis (Orphanet:108)
Bartter syndrome (Orphanet:112)
Behçet disease (Orphanet:117)
Beta-thalassemia (Orphanet:848)
Beta-thalassemia major (Orphanet:231214)
Blau syndrome (Orphanet:90340)
Blue diaper syndrome (Orphanet:94086)
Bronchiolitis obliterans with obstructive pulmonary disease (Orphanet:1303)
Budd-Chiari syndrome (Orphanet:131)
CADASIL (Orphanet:136)
CINCA syndrome (Orphanet:1451)
Caffey disease (Orphanet:1310)
Caroli disease (Orphanet:53035)
Castleman disease (Orphanet:160)
Central diabetes insipidus (Orphanet:178029)
Cholangiocarcinoma (Orphanet:70567)
Cholera (Orphanet:173)
Chronic granulomatous disease (Orphanet:379)
Chronic hiccup (Orphanet:396)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Chédiak-Higashi syndrome (Orphanet:167)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Cogan syndrome (Orphanet:1467)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Congenital primary megaureter (Orphanet:617)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cryptogenic organizing pneumonia (Orphanet:1302)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cyclic neutropenia (Orphanet:2686)
Cystinosis (Orphanet:213)
Cystinuria (Orphanet:214)
Deafness - lymphedema - leukemia (Orphanet:3226)
Dengue fever (Orphanet:99828)
Dermatomyositis (Orphanet:221)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Desquamative interstitial pneumonia (Orphanet:98852)
Distomatosis (Orphanet:1685)
Dracunculiasis (Orphanet:231)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Dubin-Johnson syndrome (Orphanet:234)
Early-onset familial noncirrhotic portal hypertension (ORPHA:494348)
Ebola hemorrhagic fever (Orphanet:319218)
Eosinophilic granuloma (Orphanet:99871)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erdheim-Chester disease (Orphanet:35687)
FEVER, FAMILIAL LIFELONG PERSISTENT (OMIM:228400)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial cold urticaria (Orphanet:47045)
Familial or sporadic hemiplegic migraine (Orphanet:569)
Fatal familial insomnia (Orphanet:466)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
Focal myositis (Orphanet:48918)
Follicular lymphoma (Orphanet:545)
Freeman-Sheldon syndrome (Orphanet:2053)
Fructose-1,6-bisphosphatase deficiency (Orphanet:348)
Gamma heavy-chain disease (Orphanet:100026)
Gaucher disease (Orphanet:355)
Gaucher disease type 2 (Orphanet:77260)
Generalized pustular psoriasis (Orphanet:247353)
Genetic recurrent myoglobinuria (Orphanet:99845)
Giant cell arteritis (Orphanet:397)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Granulomatosis with polyangiitis (Orphanet:900)
Griscelli disease (Orphanet:381)
Griscelli disease type 2 (Orphanet:79477)
HALOTHANE HEPATITIS (OMIM:234350)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3 (OMIM:608898)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 (OMIM:603552)
HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES (OMIM:239350)
HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA (OMIM:145590)
HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES (OMIM:241120)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hereditary central diabetes insipidus (Orphanet:30925)
Hereditary chronic pancreatitis (Orphanet:676)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Hodgkin lymphoma (Orphanet:98293)
Hodgkin lymphoma, classical (Orphanet:391)
Hughes-Stovin syndrome (Orphanet:228116)
Hydatidosis (Orphanet:400)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypouricemia, renal, 2 (OMIM:612076)
Idiopathic acute eosinophilic pneumonia (Orphanet:724)
Idiopathic copper-associated cirrhosis (Orphanet:209919)
Idiopathic giant cell myocarditis (Orphanet:329874)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Immunoglobulin A vasculitis (Orphanet:761)
Isolated agammaglobulinemia (Orphanet:229717)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile idiopathic arthritis (Orphanet:92)
Kawasaki disease (Orphanet:2331)
Kelley-Seegmiller syndrome (Orphanet:79233)
Kerion celsi (Orphanet:499)
King-Denborough syndrome (Orphanet:99741)
Klatskin tumor (Orphanet:99978)
Krabbe disease (Orphanet:487)
LYMPHOPROLIFERATIVE SYNDROME 2 (OMIM:615122)
Lassa fever (Orphanet:99824)
Legionellosis (Orphanet:549)
Leprechaunism (Orphanet:508)
Letterer-Siwe disease (Orphanet:99870)
Lujo hemorrhagic fever (Orphanet:319213)
Lyell syndrome (Orphanet:537)
Lyme disease (Orphanet:91546)
Lymphangioleiomyomatosis (Orphanet:538)
Lymphoid interstitial pneumonia (Orphanet:79128)
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2 (OMIM:154275)
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3 (OMIM:154276)
MELAS (Orphanet:550)
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 (OMIM:602481)
Macrophagic myofasciitis (Orphanet:592)
Majeed syndrome (Orphanet:77297)
Malakoplakia (Orphanet:556)
Malignant hyperthermia (Orphanet:423)
Marburg hemorrhagic fever (Orphanet:99826)
Marshall syndrome with periodic fever (Orphanet:42642)
Melkersson-Rosenthal syndrome (Orphanet:2483)
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency (Orphanet:319600)
Microscopic polyangiitis (Orphanet:727)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Mixed connective tissue disease (Orphanet:809)
Mixed-type autoimmune hemolytic anemia (Orphanet:90036)
Moderate multiminicore disease with hand involvement (Orphanet:178145)
Muckle-Wells syndrome (Orphanet:575)
Multicentric reticulohistiocytosis (Orphanet:139436)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Nakajo-Nishimura syndrome (Orphanet:2615)
Nephroblastoma (Orphanet:654)
Neuroblastoma (Orphanet:635)
Nipah virus disease (Orphanet:99825)
Nodular lymphocyte predominant Hodgkin lymphoma (Orphanet:86893)
Nodular non-suppurative panniculitis (Orphanet:33577)
Non-specific interstitial pneumonia (Orphanet:91364)
Omenn syndrome (Orphanet:39041)
Osteopetrosis (Orphanet:2781)
PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT (OMIM:614674)
Paroxysmal cold hemoglobinuria (Orphanet:90035)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Peripartum cardiomyopathy (Orphanet:563)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polymyositis (Orphanet:732)
Pontiac fever (Orphanet:99748)
Porphyria (Orphanet:738)
Primary cutaneous lymphoma (Orphanet:542)
Progressive nodular histiocytosis (Orphanet:158022)
Pseudodiastrophic dysplasia (Orphanet:85174)
Pulmonary blastoma (Orphanet:64741)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pyogenic arthritis - pyoderma gangrenosum - acne (Orphanet:69126)
Pyogenic bacterial infections due to MyD88 deficiency (Orphanet:183713)
Pyomyositis (Orphanet:764)
Rabies (Orphanet:770)
Reactive arthritis (Orphanet:29207)
Relapsing polychondritis (Orphanet:728)
Reticular dysgenesis (Orphanet:33355)
Reynolds syndrome (Orphanet:779)
Rhabdoid tumor (Orphanet:69077)
Rheumatic fever (Orphanet:3099)
Rift valley fever (Orphanet:319251)
Rosaï-Dorfman disease (Orphanet:158014)
Rotor syndrome (Orphanet:3111)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Sarcoidosis (Orphanet:797)
Schnitzler syndrome (Orphanet:37748)
Scrub typhus (Orphanet:83317)
Severe combined immunodeficiency (Orphanet:183660)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Stevens-Johnson syndrome (Orphanet:36426)
Stiff person syndrome (Orphanet:3198)
Susceptibility to chronic infection by Epstein-Barr virus (Orphanet:2566)
Sweet syndrome (Orphanet:3243)
Systemic capillary leak syndrome (Orphanet:188)
Systemic-onset juvenile idiopathic arthritis (Orphanet:85414)
Sézary syndrome (Orphanet:3162)
TRAPS syndrome (Orphanet:32960)
Takayasu arteritis (Orphanet:3287)
Thiamine-responsive encephalopathy (Orphanet:199348)
Thrombotic thrombocytopenic purpura (Orphanet:54057)
Typhoid (Orphanet:99745)
Viral hemorrhagic fever (Orphanet:341)
Waldenström macroglobulinemia (Orphanet:33226)
Whipple disease (Orphanet:3452)
Wiskott-Aldrich syndrome (Orphanet:906)
Wolman disease (Orphanet:75233)
Wound botulism (Orphanet:178475)
X-linked agammaglobulinemia (Orphanet:47)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
X-linked lymphoproliferative disease (Orphanet:2442)
Xeroderma pigmentosum (Orphanet:910)
Yellow fever (Orphanet:99829)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)