Malaria

A life-threatening parasitic disease caused by <i>Plasmodium</i> (<i>P. </i>) parasites that are transmitted by <i>Anophles</i> mosquito bites to humans and is typically clinically characterized by attacks of fever, headache, chills and vomiting.



Input patient's signs and symptoms


Narrow down the case reports



Total: 1234 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(62.6%)
16562788
A rare cause of anemia and thrombocytopenia in a newborn: congenital malaria.
Baspinar O, Bayraktaroglu Z, Karsligil T, Bayram A, Coskun Y.
Turk J Pediatr. 2006;48(1):63-5.
Jaundice Splenomegaly Anemia Fever
Adult Anemia Females Homo sapiens Infant, Newborn Malaria Pregnancy Pregnancy Complications, Infectious Thrombocytopenia
1
(62.6%)
15900844
[A transfusion-transmitted malaria case].
Ozkurt Z, Erol S, Kadanali A, Altoparlak U, Tasyaran MA.
Mikrobiyol Bul. 2005;39(1):101-5.
Jaundice Splenomegaly Anemia Fever
Animals Antimalarials Chills Diarrhea Females Fever Homo sapiens Icterus Malaria, Vivax Middle Aged Plasmodium vivax Splenomegaly Transfusion Reaction Vomiting
3
(60.6%)
24251259
(3830150)
Congenital malaria with atypical presentation in a preterm neonate.
Kumar R, Kumar K.
J Clin Neonatol. 2013;2(3):138-9.
Jaundice Hepatosplenomegaly Anemia Fever
3
(60.6%)
1677409
[Imported case of malaria in Taiwan: analysis of 11 cases].
Lin SY, Tzeng SH, Chang YM, Siauw CP, Chen PH.
J Formos Med Assoc. 1991;90(3):308-11.
Jaundice Hepatosplenomegaly Anemia Fever
G6PD
Adult Homo sapiens Malaria Male Middle Aged Taiwan
5
(56.2%)
29111186
Plasmodium falciparum found in the bone marrow of a child in Manado City, East Indonesia: A case report.
Tatura SNN, Gunawan S, Bernadus J, Sandjoto S.
Asian Pac J Trop Med. 2017;10(10):1015-1017.
Splenomegaly Anemia Fever
5
(56.2%)
26488102
[13-year old girl with fever 6 months after returning from sub-Saharan Africa].
Erhardt J, Frank M.
Dtsch Med Wochenschr. 2015;140(21):1614.
Splenomegaly Anemia Fever
G6PD HP
Africa Developing Countries Females Fever of Unknown Origin Germany Homo sapiens Malaria Plasmodium ovale
5
(56.2%)
10890139
[Congenital malaria due to Plasmodium falciparum and Plasmodium malariae].
Zenz W, Trop M, Kollaritsch H, Reinthaler F.
Wien Klin Wochenschr. 2000;112(10):459-61.
Splenomegaly Hemolytic anemia Fever
Adult Animals Antimalarials Austria Females Fever of Unknown Origin Ghana Homo sapiens Infant Malaria Malaria, Falciparum Male Plasmodium falciparum Plasmodium malariae Time Factors
5
(56.2%)
9503898
A review of 79 patients with malaria seen at a military hospital in Hawaii from 1979 to 1995.
Kortepeter M, Brown JD.
Mil Med. 1998;163(2):84-9.
Splenomegaly Anemia Fever
Adult Differential Diagnosis Emigration and Immigration Females Hawaii Homo sapiens Malaria, Falciparum Malaria, Vivax Male Middle Aged Military Hospitals Military Personnel
5
(56.2%)
2509594
[A case of Plasmodium vivax malaria complicated with pancytopenia due to hypoplasia of the bone marrow].
Yamakawa H, Kiyotaki M, Hattori Y, Obana M, Matsuoka Y, Irimajiri S.
Kansenshogaku Zasshi. 1989;63(9):1043-6.
Splenomegaly Anemia Fever
Adult Animals Bone Marrow Homo sapiens Malaria Male Pancytopenia Plasmodium vivax
5
(56.2%)
1576289
Congenital malaria in the United States: report of a case and review.
Hulbert TV.
Clin Infect Dis. 1992;14(4):922-6.
Splenomegaly Anemia Fever
Adult Females Guatemala Homo sapiens Infant Malaria Pregnancy United States
        

Phenotype(s) retrieved from Orphanet

    Total: 16

HPO ID Term Frequency
HP:0001903 Anemia Very frequent (99-80%)
HP:0001919 Acute kidney injury Very frequent (99-80%)
HP:0001945 Fever Very frequent (99-80%)
HP:0002011 Morphological abnormality of the central nervous system Very frequent (99-80%)
HP:0002017 Nausea and vomiting Very frequent (99-80%)
HP:0002315 Headache Very frequent (99-80%)
HP:0011227 Elevated C-reactive protein level Very frequent (99-80%)
HP:0001871 Abnormality of blood and blood-forming tissues Frequent (79-30%)
HP:0001873 Thrombocytopenia Frequent (79-30%)
HP:0002098 Respiratory distress Frequent (79-30%)
HP:0002141 Gait imbalance Frequent (79-30%)
HP:0002904 Hyperbilirubinemia Frequent (79-30%)
HP:0003326 Myalgia Frequent (79-30%)
HP:0004372 Reduced consciousness/confusion Frequent (79-30%)
HP:0100543 Cognitive impairment Frequent (79-30%)
HP:0000488 Retinopathy Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 259

HPO ID Term # of case reports
HP:0001945 Fever 207
HP:0001873 Thrombocytopenia 55
HP:0002098 Respiratory distress 51
HP:0001744 Splenomegaly 31
HP:0001903 Anemia 29
HP:0031273 Shock 28
HP:0000952 Jaundice 27
HP:0005521 Disseminated intravascular coagulation 25
HP:0012223 Splenic rupture 21
HP:0001298 Encephalopathy 20
HP:0001250 Seizures 19
HP:0025143 Chills 17
HP:0100598 Pulmonary edema 17
HP:0012115 Hepatitis 15
HP:0100758 Gangrene 15
HP:0100806 Sepsis 14
HP:0002315 Headache 13
HP:0001876 Pancytopenia 12
HP:0001919 Acute kidney injury 12
HP:0002090 Pneumonia 10
HP:0000488 Retinopathy 9
HP:0001251 Ataxia 9
HP:0001735 Acute pancreatitis 9
HP:0012819 Myocarditis 9
HP:0000979 Purpura 8
HP:0001287 Meningitis 8
HP:0001289 Confusion 8
HP:0001943 Hypoglycemia 8
HP:0002013 Vomiting 8
HP:0006562 Viral hepatitis 8
HP:0000083 Renal insufficiency 7
HP:0000709 Psychosis 7
HP:0001942 Metabolic acidosis 7
HP:0002027 Abdominal pain 7
HP:0000099 Glomerulonephritis 6
HP:0001082 Cholecystitis 6
HP:0001878 Hemolytic anemia 6
HP:0003201 Rhabdomyolysis 6
HP:0031864 Bacteremia 6
HP:0040187 Neonatal sepsis 6
HP:0001370 Rheumatoid arthritis 5
HP:0001433 Hepatosplenomegaly 5
HP:0002014 Diarrhea 5
HP:0002018 Nausea 5
HP:0002904 Hyperbilirubinemia 5
HP:0003641 Hemoglobinuria 5
HP:0005575 Hemolytic-uremic syndrome 5
HP:0011675 Arrhythmia 5
HP:0012378 Fatigue 5
HP:0001271 Polyneuropathy 4
HP:0001955 Unexplained fevers 4
HP:0002615 Hypotension 4
HP:0002721 Immunodeficiency 4
HP:0003470 Paralysis 4
HP:0012156 Hemophagocytosis 4
HP:0012234 Agranulocytosis 4
HP:0025145 Rigors 4
HP:0025615 Abscess 4
HP:0030731 Carcinoma 4
HP:0032169 Severe infection 4
HP:0000112 Nephropathy 3
HP:0000572 Visual loss 3
HP:0000573 Retinal hemorrhage 3
HP:0000618 Blindness 3
HP:0001658 Myocardial infarction 3
HP:0001909 Leukemia 3
HP:0001941 Acidosis 3
HP:0001954 Recurrent fever 3
HP:0002240 Hepatomegaly 3
HP:0002754 Osteomyelitis 3
HP:0002878 Respiratory failure 3
HP:0002902 Hyponatremia 3
HP:0004395 Malnutrition 3
HP:0011854 Hemoperitoneum 3
HP:0025418 Renal cortical necrosis 3
HP:0200119 Acute hepatitis 3
HP:0000100 Nephrotic syndrome 2
HP:0000238 Hydrocephalus 2
HP:0000725 Psychotic episodes 2
HP:0000969 Edema 2
HP:0000989 Pruritus 2
HP:0001025 Urticaria 2
HP:0001297 Stroke 2
HP:0001336 Myoclonus 2
HP:0001337 Tremor 2
HP:0001396 Cholestasis 2
HP:0001399 Hepatic failure 2
HP:0001649 Tachycardia 2
HP:0001733 Pancreatitis 2
HP:0001875 Neutropenia 2
HP:0001880 Eosinophilia 2
HP:0002045 Hypothermia 2
HP:0002133 Status epilepticus 2
HP:0002527 Falls 2
HP:0002588 Duodenal ulcer 2
HP:0002900 Hypokalemia 2
HP:0002913 Myoglobinuria 2
HP:0003074 Hyperglycemia 2
HP:0003326 Myalgia 2
HP:0005523 Lymphoproliferative disorder 2
HP:0008682 Acute tubular necrosis 2
HP:0008765 Auditory hallucinations 2
HP:0010444 Pulmonary insufficiency 2
HP:0012330 Pyelonephritis 2
HP:0020101 Invasive fungal infection 2
HP:0025059 Splenic abscess 2
HP:0025502 Overweight 2
HP:0025574 Macular hemorrhage 2
HP:0030955 Alcoholism 2
HP:0031258 Delirium 2
HP:0031690 Opportunistic infection 2
HP:0032252 Granuloma 2
HP:0040075 Hypopituitarism 2
HP:0100584 Endocarditis 2
HP:0100749 Chest pain 2
HP:0000021 Megacystis 1
HP:0000103 Polyuria 1
HP:0000126 Hydronephrosis 1
HP:0000225 Gingival bleeding 1
HP:0000246 Sinusitis 1
HP:0000360 Tinnitus 1
HP:0000491 Keratitis 1
HP:0000597 Ophthalmoparesis 1
HP:0000603 Central scotoma 1
HP:0000713 Agitation 1
HP:0000717 Autism 1
HP:0000718 Aggressive behavior 1
HP:0000737 Irritability 1
HP:0000738 Hallucinations 1
HP:0000787 Nephrolithiasis 1
HP:0000793 Membranoproliferative glomerulonephritis 1
HP:0000819 Diabetes mellitus 1
HP:0000822 Hypertension 1
HP:0000846 Adrenal insufficiency 1
HP:0000939 Osteoporosis 1
HP:0000961 Cyanosis 1
HP:0000980 Pallor 1
HP:0001019 Erythroderma 1
HP:0001085 Papilledema 1
HP:0001138 Optic neuropathy 1
HP:0001269 Hemiparesis 1
HP:0001272 Cerebellar atrophy 1
HP:0001281 Tetany 1
HP:0001300 Parkinsonism 1
HP:0001369 Arthritis 1
HP:0001409 Portal hypertension 1
HP:0001511 Intrauterine growth retardation 1
HP:0001541 Ascites 1
HP:0001562 Oligohydramnios 1
HP:0001622 Premature birth 1
HP:0001638 Cardiomyopathy 1
HP:0001657 Prolonged QT interval 1
HP:0001695 Cardiac arrest 1
HP:0001698 Pericardial effusion 1
HP:0001701 Pericarditis 1
HP:0001806 Onycholysis 1
HP:0001824 Weight loss 1
HP:0001888 Lymphopenia 1
HP:0001889 Megaloblastic anemia 1
HP:0001892 Abnormal bleeding 1
HP:0001895 Normochromic anemia 1
HP:0001897 Normocytic anemia 1
HP:0001913 Granulocytopenia 1
HP:0001923 Reticulocytosis 1
HP:0001937 Microangiopathic hemolytic anemia 1
HP:0001944 Dehydration 1
HP:0001971 Hypersplenism 1
HP:0001972 Macrocytic anemia 1
HP:0001993 Ketoacidosis 1
HP:0002017 Nausea and vomiting 1
HP:0002063 Rigidity 1
HP:0002093 Respiratory insufficiency 1
HP:0002099 Asthma 1
HP:0002105 Hemoptysis 1
HP:0002113 Pulmonary infiltrates 1
HP:0002179 Opisthotonus 1
HP:0002181 Cerebral edema 1
HP:0002202 Pleural effusion 1
HP:0002204 Pulmonary embolism 1
HP:0002206 Pulmonary fibrosis 1
HP:0002239 Gastrointestinal hemorrhage 1
HP:0002249 Melena 1
HP:0002310 Orofacial dyskinesia 1
HP:0002329 Drowsiness 1
HP:0002381 Aphasia 1
HP:0002385 Paraparesis 1
HP:0002480 Hepatic encephalopathy 1
HP:0002516 Increased intracranial pressure 1
HP:0002617 Dilatation 1
HP:0002621 Atherosclerosis 1
HP:0002664 Neoplasm 1
HP:0002716 Lymphadenopathy 1
HP:0002719 Recurrent infections 1
HP:0002751 Kyphoscoliosis 1
HP:0002827 Hip dislocation 1
HP:0002829 Arthralgia 1
HP:0002840 Lymphadenitis 1
HP:0002960 Autoimmunity 1
HP:0003072 Hypercalcemia 1
HP:0003146 Hypocholesterolemia 1
HP:0004322 Short stature 1
HP:0004398 Peptic ulcer 1
HP:0004755 Supraventricular tachycardia 1
HP:0004787 Fulminant hepatitis 1
HP:0004948 Vascular tortuosity 1
HP:0005214 Intestinal obstruction 1
HP:0005268 Spontaneous abortion 1
HP:0005305 Cerebral venous thrombosis 1
HP:0005659 Thoracic kyphoscoliosis 1
HP:0006532 Recurrent pneumonia 1
HP:0006689 Bacterial endocarditis 1
HP:0006846 Acute encephalopathy 1
HP:0007024 Pseudobulbar paralysis 1
HP:0007185 Loss of consciousness 1
HP:0008940 Generalized lymphadenopathy 1
HP:0009830 Peripheral neuropathy 1
HP:0010543 Opsoclonus 1
HP:0011002 Osteopetrosis 1
HP:0011106 Hypovolemia 1
HP:0011504 Bull's eye maculopathy 1
HP:0011947 Respiratory tract infection 1
HP:0011999 Paranoia 1
HP:0012119 Methemoglobinemia 1
HP:0012219 Erythema nodosum 1
HP:0012311 Monocytosis 1
HP:0012418 Hypoxemia 1
HP:0012424 Chorioretinitis 1
HP:0012531 Pain 1
HP:0012735 Cough 1
HP:0025044 Lung abscess 1
HP:0025085 Bloody diarrhea 1
HP:0025144 Shivering 1
HP:0025289 Cervical lymphadenopathy 1
HP:0025435 Increased lactate dehydrogenase activity 1
HP:0030764 Ochronosis 1
HP:0030915 Cerebellar edema 1
HP:0031284 Flushing 1
HP:0031803 Fundus hemorrhage 1
HP:0031805 Intraretinal hemorrhage 1
HP:0031931 Ocular flutter 1
HP:0032160 Cryptococcal meningitis 1
HP:0032255 Opportunistic fungal infection 1
HP:0032323 Periodic fever 1
HP:0040318 Red urine 1
HP:0100520 Oliguria 1
HP:0100523 Liver abscess 1
HP:0100543 Cognitive impairment 1
HP:0100614 Myositis 1
HP:0100633 Esophagitis 1
HP:0100653 Optic neuritis 1
HP:0100658 Cellulitis 1
HP:0100718 Uterine rupture 1
HP:0100754 Mania 1
HP:0100820 Glomerulopathy 1
HP:0100827 Lymphocytosis 1
HP:0200023 Priapism 1
HP:0200085 Limb tremor 1
HP:0200123 Chronic hepatitis 1
HP:0410019 Epigastric pain 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID