Fever
Symptom Information:
Symptom ID: | HPO:0001945 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||||||||||||||||||||
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: Investigations(MedDRA:10022891) Physical examination and organ system status topics(MedDRA:10071940) Physical examination procedures and organ system status(MedDRA:10071941) 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) General disorders and administration site conditions(MedDRA:10018065) Body temperature conditions(MedDRA:10005908) Febrile disorders(MedDRA:10016286) Fever(HPO:0001945) |
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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) |