Typhoid

Typhoid or typhoid fever is a reportable, fecal-oral, potentially fatal infectious disease, caused by the bacteria <i>Salmonella typhi</i> and characterized by a non-focal fever.



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Narrow down the case reports



Total: 397 (papers)

   


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
370
(5.0%)		 2517555
 Paratyphoid fever presenting with renal failure and nephrotic syndrome.
Onwubalili JK.
Trop Geogr Med. 1989;41(4):368-71.
Nephrotic syndrome
Adult Females Homo sapiens Nephrotic Syndrome Nigeria Paratyphoid Fever Salmonella paratyphi B
370
(5.0%)		 2289513
 Pseudotumor cerebri complicating typhoid fever.
Vargas JA, Garcia-Merino A, Rodriguez E, Villagra A.
Eur Neurol. 1990;30(6):345-6.
Headache
Adult Females Homo sapiens Pseudotumor Cerebri Typhoid Fever
370
(5.0%)		 1875582
 [A case of pleuritis tuberculosa which was diagnosed as inoculated tuberculosis after 43 years].
Tamura M.
Kekkaku. 1991;66(5):395-8.
Pleuritis
Females Homo sapiens Middle Aged Pleural Tuberculosis Time Factors Vaccination
370
(5.0%)		 1404563
 Typhoid fever and nephrotic syndrome--an unusual association.
Karthikeyan G, Nalini P.
J Trop Med Hyg. 1992;95(5):356-7.
Nephrotic syndrome
Child Homo sapiens Male Nephrotic Syndrome Typhoid Fever
370
(5.0%)		 1341094
 Quinine blindness.
Naraqi S, Okem S, Moyia N, Dutta TK, Zzferio B, Lalloo D.
P N G Med J. 1992;35(4):308-10.
Blindness
Adult Blindness Combination Drug Therapy Females Homo sapiens Malaria Ophthalmoscopy Referral and Consultation Typhoid Fever Visual Acuity
370
(5.0%)		 1235006
 [Typhoid encefalopathy followed by permanent memory defects (author's transl)].
Nichelli P, Spinnler H.
Riv Patol Nerv Ment. 1975;96(5):301-7.
Mental deterioration
Acute Disease Brain Diseases Females Homo sapiens Memory Disorders Speech Disorders Typhoid Fever
370
(5.0%)		 598125
 Salmonella spondylitis. Report of 2 cases.
Mnaymneh W.
Clin Orthop Relat Res. 1977;(126):235-8.
Paraparesis
Differential Diagnosis Females Homo sapiens Male Middle Aged Spondylitis Tuberculosis, Spinal
        

Phenotype(s) retrieved from Orphanet

    Total: 27

HPO ID Term Frequency
HP:0001945 Fever Very frequent (99-80%)
HP:0002027 Abdominal pain Very frequent (99-80%)
HP:0002315 Headache Very frequent (99-80%)
HP:0012378 Fatigue Very frequent (99-80%)
HP:0100785 Insomnia Very frequent (99-80%)
HP:0000988 Skin rash Frequent (79-30%)
HP:0001251 Ataxia Frequent (79-30%)
HP:0001276 Hypertonia Frequent (79-30%)
HP:0001347 Hyperreflexia Frequent (79-30%)
HP:0001744 Splenomegaly Frequent (79-30%)
HP:0002240 Hepatomegaly Frequent (79-30%)
HP:0002829 Arthralgia Frequent (79-30%)
HP:0003326 Myalgia Frequent (79-30%)
HP:0011675 Arrhythmia Frequent (79-30%)
HP:0012733 Macule Frequent (79-30%)
HP:0000421 Epistaxis Occasional (29-5%)
HP:0001254 Lethargy Occasional (29-5%)
HP:0001259 Coma Occasional (29-5%)
HP:0001337 Tremor Occasional (29-5%)
HP:0001695 Cardiac arrest Occasional (29-5%)
HP:0002014 Diarrhea Occasional (29-5%)
HP:0002019 Constipation Occasional (29-5%)
HP:0002239 Gastrointestinal hemorrhage Occasional (29-5%)
HP:0002383 Encephalitis Occasional (29-5%)
HP:0004936 Venous thrombosis Occasional (29-5%)
HP:0006530 Interstitial pulmonary abnormality Occasional (29-5%)
HP:0012735 Cough Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 147

HPO ID Term # of case reports
HP:0001945 Fever 56
HP:0012115 Hepatitis 30
HP:0001287 Meningitis 14
HP:0012819 Myocarditis 11
HP:0000952 Jaundice 9
HP:0025615 Abscess 9
HP:0031864 Bacteremia 9
HP:0100806 Sepsis 9
HP:0100584 Endocarditis 8
HP:0001082 Cholecystitis 7
HP:0002586 Peritonitis 7
HP:0006562 Viral hepatitis 7
HP:0025059 Splenic abscess 7
HP:0001735 Acute pancreatitis 6
HP:0001873 Thrombocytopenia 6
HP:0002583 Colitis 6
HP:0002014 Diarrhea 5
HP:0031368 Intestinal perforation 5
HP:0001298 Encephalopathy 4
HP:0001744 Splenomegaly 4
HP:0002013 Vomiting 4
HP:0002027 Abdominal pain 4
HP:0002090 Pneumonia 4
HP:0002098 Respiratory distress 4
HP:0002240 Hepatomegaly 4
HP:0002721 Immunodeficiency 4
HP:0003095 Septic arthritis 4
HP:0005661 Salmonella osteomyelitis 4
HP:0031258 Delirium 4
HP:0000099 Glomerulonephritis 3
HP:0000709 Psychosis 3
HP:0001251 Ataxia 3
HP:0001369 Arthritis 3
HP:0001662 Bradycardia 3
HP:0001733 Pancreatitis 3
HP:0001824 Weight loss 3
HP:0001876 Pancytopenia 3
HP:0002202 Pleural effusion 3
HP:0002615 Hypotension 3
HP:0002754 Osteomyelitis 3
HP:0005521 Disseminated intravascular coagulation 3
HP:0012330 Pyelonephritis 3
HP:0031273 Shock 3
HP:0200119 Acute hepatitis 3
HP:0000123 Nephritis 2
HP:0000822 Hypertension 2
HP:0001081 Cholelithiasis 2
HP:0001433 Hepatosplenomegaly 2
HP:0001903 Anemia 2
HP:0002019 Constipation 2
HP:0002315 Headache 2
HP:0002840 Lymphadenitis 2
HP:0003201 Rhabdomyolysis 2
HP:0006689 Bacterial endocarditis 2
HP:0012219 Erythema nodosum 2
HP:0012223 Splenic rupture 2
HP:0032252 Granuloma 2
HP:0100523 Liver abscess 2
HP:0100646 Thyroiditis 2
HP:0100658 Cellulitis 2
HP:0100758 Gangrene 2
HP:0000027 Azoospermia 1
HP:0000093 Proteinuria 1
HP:0000100 Nephrotic syndrome 1
HP:0000112 Nephropathy 1
HP:0000126 Hydronephrosis 1
HP:0000282 Facial edema 1
HP:0000488 Retinopathy 1
HP:0000746 Delusions 1
HP:0000819 Diabetes mellitus 1
HP:0000821 Hypothyroidism 1
HP:0000961 Cyanosis 1
HP:0000969 Edema 1
HP:0000970 Anhidrosis 1
HP:0001250 Seizures 1
HP:0001289 Confusion 1
HP:0001300 Parkinsonism 1
HP:0001370 Rheumatoid arthritis 1
HP:0001399 Hepatic failure 1
HP:0001645 Sudden cardiac death 1
HP:0001875 Neutropenia 1
HP:0001919 Acute kidney injury 1
HP:0001970 Tubulointerstitial nephritis 1
HP:0002039 Anorexia 1
HP:0002045 Hypothermia 1
HP:0002170 Intracranial hemorrhage 1
HP:0002239 Gastrointestinal hemorrhage 1
HP:0002305 Athetosis 1
HP:0002381 Aphasia 1
HP:0002427 Motor aphasia 1
HP:0002527 Falls 1
HP:0002576 Intussusception 1
HP:0002584 Intestinal bleeding 1
HP:0002716 Lymphadenopathy 1
HP:0002878 Respiratory failure 1
HP:0002901 Hypocalcemia 1
HP:0002902 Hyponatremia 1
HP:0002907 Microscopic hematuria 1
HP:0002913 Myoglobinuria 1
HP:0003198 Myopathy 1
HP:0003249 Genital ulcers 1
HP:0003270 Abdominal distention 1
HP:0003326 Myalgia 1
HP:0003470 Paralysis 1
HP:0004398 Peptic ulcer 1
HP:0004787 Fulminant hepatitis 1
HP:0004804 Congenital hemolytic anemia 1
HP:0005180 Tricuspid regurgitation 1
HP:0005575 Hemolytic-uremic syndrome 1
HP:0006846 Acute encephalopathy 1
HP:0007430 Generalized edema 1
HP:0008198 Congenital hypoparathyroidism 1
HP:0008682 Acute tubular necrosis 1
HP:0009792 Teratoma 1
HP:0010550 Paraplegia 1
HP:0010783 Erythema 1
HP:0010818 Generalized tonic seizures 1
HP:0011704 Sick sinus syndrome 1
HP:0011947 Respiratory tract infection 1
HP:0012089 Arteritis 1
HP:0012156 Hemophagocytosis 1
HP:0012387 Bronchitis 1
HP:0012418 Hypoxemia 1
HP:0012424 Chorioretinitis 1
HP:0012461 Bacteriuria 1
HP:0012735 Cough 1
HP:0025143 Chills 1
HP:0025343 Lupus anticoagulant 1
HP:0030049 Brain abscess 1
HP:0030154 Gallbladder perforation 1
HP:0030451 Mesenteric cyst 1
HP:0030995 Peritoneal effusion 1
HP:0031003 Polyneuritis 1
HP:0031179 Nuchal rigidity 1
HP:0031369 Colon perforation 1
HP:0031456 Ectopic pregnancy 1
HP:0031500 Abdominal mass 1
HP:0031925 Rosette 1
HP:0032118 Retinitis 1
HP:0040187 Neonatal sepsis 1
HP:0100520 Oliguria 1
HP:0100614 Myositis 1
HP:0100754 Mania 1
HP:0100796 Orchitis 1
HP:0100845 Anaphylactic shock 1
HP:0200036 Skin nodule 1
HP:0200123 Chronic hepatitis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID