Hemophilia A

Hemophilia A is the most common form of hemophilia (see this term) characterized by spontaneous or prolonged hemorrhages due to factor VIII deficiency.



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Narrow down the case reports



Total: 409 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(49.1%)
8745824
[Severe parvovirus B19 infection in an immunocompetent child with hemophilia A].
Coumau E, Peynet J, Harzic M, Beal G, Castaigne S, Leverger G, Foucaud P.
Arch Pediatr. 1996;3(1):35-9.
Anemia Fever Erythema
Anticoagulants Child Drug Contamination Erythema Infectiosum Hemophilia A Homo sapiens Immunocompetence Male Retrospective Studies
2
(47.4%)
26157867
(4435321)
Delayed Presentation of Splenic Rupture After Endoscopy in a Patient With Hemophilia A: Case Report and Review of the Literature.
Mazulis A, Lakha A, Qazi B, Shapiro A.
ACG Case Rep J. 2014;1(4):175-7.
Anemia Hemoperitoneum Splenic rupture
2
(47.4%)
20404752
Splenic rupture in a newborn with severe hemophilia--case report and review.
Tengsupakul S, Sedrak A, Freed J, Martinez-Carde L, Fireman F, Pierre L, Sadanandan S.
J Pediatr Hematol Oncol. 2010;32(4):323-6.
Anemia Hemoperitoneum Splenic rupture
Adult Females Hemophilia A Homo sapiens Infant, Newborn Male Splenic Rupture X-Ray Computed Tomography
2
(47.4%)
16952601
Nonoperative management of delayed splenic rupture in a patient with hemophilia B.
Terry NE, Boswell WC.
J Pediatr Surg. 2006;41(9):1607-9.
Anemia Splenic rupture
COX8A
Hemophilia B Hemorrhage Homo sapiens Hypotension Male Recombinant Proteins Skating Splenic Rupture Time Factors
5
(44.2%)
7564051
[Massive and progressive hepatosplenomegaly caused by disseminated nontuberculous mycobacteriosis in a patient with acquired immunodeficiency syndrome].
Hagiwara T, Amano K, Sugimura D, Isogai N, Arai M, Fukutake K, Kojima H, Shimada H.
Kekkaku. 1995;70(7):423-9.
Hepatosplenomegaly Pancytopenia Fever
CD4
AIDS-Related Opportunistic Infections Acquired Immunodeficiency Syndrome Adult Hemophilia A Hepatomegaly Homo sapiens Male Mycobacterium avium Complex Mycobacterium avium-intracellulare Infection Polymerase Chain Reaction Splenomegaly
6
(42.9%)
27885231
Two elderly patients with difficult-to-treat acquired hemophilia A.
Saito M, Morioka M.
Nihon Ronen Igakkai Zasshi. 2016;53(4):424-430.
Anemia Subcutaneous hemorrhage
Aged, 80 and over Females Hemophilia A Hemorrhage Homo sapiens Immunosuppressive Agents
6
(42.9%)
22301942
Acquired hemophilia A in a patient with essential thrombocythemia.
Mori N, Totsuka K, Ishimori N, Yoshinaga K, Teramura M, Noguchi S, Oda H, Motoji T.
Acta Haematol. 2012;127(3):170-2.
Anemia Ecchymosis
COX8A
Cerebral Infarction Ecchymosis Females Hemophilia A Homo sapiens Thrombocythemia, Essential X-Ray Computed Tomography
8
(42.5%)
6226910
DDAVP: review of indications for its use in the treatment of factor VIII deficiency and report of a case.
Eastman JR, Nowakowski AR, Triplett DA.
Oral Surg Oral Med Oral Pathol. 1983;56(3):246-51.
Hemolytic anemia Hepatitis
Adult Dental Care for Disabled Drug Combinations Hemophilia A Homo sapiens Male Oral Hemorrhage Oral Surgical Procedures, Preprosthetic
9
(42.5%)
24568115
Hemorrhage and blood loss-induced anemia associated with an acquired coagulation factor VIII inhibitor in a Thoroughbred mare.
Winfield LS, Brooks MB.
J Am Vet Med Assoc. 2014;244(6):719-23.
Pallor Anemia Hemoperitoneum
Animals Blood Transfusion Equus caballus Females Hemophilia A Horse Diseases
10
(38.7%)
12474336
Small dose of recombinant factor VIIa (rFVIIa) to perform percutaneous liver biopsies in cirrhotic patients.
Carvalho A, Leitao J, Louro E, Maia R, Geraldes C, Ventura C, Silvestre M, Porto A.
Rev Esp Enferm Dig. 2002;94(5):280-5.
Cirrhosis Low levels of vitamin K
Adult Biopsy Blood Coagulation Disorders Homo sapiens Liver Cirrhosis Male Middle Aged Preoperative Care Recombinant Proteins
        

Phenotype(s) retrieved from Orphanet

    Total: 14

HPO ID Term Frequency
HP:0001386 Joint swelling Very frequent (99-80%)
HP:0002829 Arthralgia Very frequent (99-80%)
HP:0003125 Reduced factor VIII activity Very frequent (99-80%)
HP:0011889 Bleeding with minor or no trauma Very frequent (99-80%)
HP:0001907 Thromboembolism Frequent (79-30%)
HP:0007420 Spontaneous hematomas Frequent (79-30%)
HP:0030140 Oral cavity bleeding Frequent (79-30%)
HP:0002239 Gastrointestinal hemorrhage Occasional (29-5%)
HP:0005261 Joint hemorrhage Occasional (29-5%)
HP:0009811 Abnormality of the elbow Occasional (29-5%)
HP:0012233 Intramuscular hematoma Occasional (29-5%)
HP:0030746 Intraventricular hemorrhage Occasional (29-5%)
HP:0002170 Intracranial hemorrhage Very rare (4-1%)
HP:0012223 Splenic rupture Very rare (4-1%)


Phenotype(s) retrieved from case reports

    Total: 139

HPO ID Term # of case reports
HP:0001658 Myocardial infarction 8
HP:0001909 Leukemia 8
HP:0012115 Hepatitis 8
HP:0001394 Cirrhosis 7
HP:0002721 Immunodeficiency 7
HP:0001945 Fever 5
HP:0031273 Shock 5
HP:0000790 Hematuria 4
HP:0000819 Diabetes mellitus 4
HP:0001370 Rheumatoid arthritis 4
HP:0002090 Pneumonia 4
HP:0000737 Irritability 3
HP:0000979 Purpura 3
HP:0005521 Disseminated intravascular coagulation 3
HP:0012223 Splenic rupture 3
HP:0031625 Pseudoaneurysm 3
HP:0000100 Nephrotic syndrome 2
HP:0000421 Epistaxis 2
HP:0000518 Cataract 2
HP:0001541 Ascites 2
HP:0001735 Acute pancreatitis 2
HP:0001933 Subcutaneous hemorrhage 2
HP:0002013 Vomiting 2
HP:0002107 Pneumothorax 2
HP:0002170 Intracranial hemorrhage 2
HP:0002315 Headache 2
HP:0002527 Falls 2
HP:0002758 Osteoarthritis 2
HP:0003010 Prolonged bleeding time 2
HP:0003040 Arthropathy 2
HP:0003645 Prolonged partial thromboplastin time 2
HP:0012125 Prostate cancer 2
HP:0012233 Intramuscular hematoma 2
HP:0030731 Carcinoma 2
HP:0040184 Oral bleeding 2
HP:0100279 Ulcerative colitis 2
HP:0200123 Chronic hepatitis 2
HP:0000126 Hydronephrosis 1
HP:0000133 Gonadal dysgenesis 1
HP:0000225 Gingival bleeding 1
HP:0000238 Hydrocephalus 1
HP:0000388 Otitis media 1
HP:0000501 Glaucoma 1
HP:0000726 Dementia 1
HP:0000771 Gynecomastia 1
HP:0000787 Nephrolithiasis 1
HP:0000822 Hypertension 1
HP:0000952 Jaundice 1
HP:0000969 Edema 1
HP:0000980 Pallor 1
HP:0001031 Subcutaneous lipoma 1
HP:0001289 Confusion 1
HP:0001298 Encephalopathy 1
HP:0001342 Cerebral hemorrhage 1
HP:0001369 Arthritis 1
HP:0001482 Subcutaneous nodule 1
HP:0001513 Obesity 1
HP:0001629 Ventricular septal defect 1
HP:0001638 Cardiomyopathy 1
HP:0001649 Tachycardia 1
HP:0001650 Aortic valve stenosis 1
HP:0001681 Angina pectoris 1
HP:0001701 Pericarditis 1
HP:0001733 Pancreatitis 1
HP:0001742 Nasal obstruction 1
HP:0001873 Thrombocytopenia 1
HP:0001875 Neutropenia 1
HP:0001876 Pancytopenia 1
HP:0001891 Iron deficiency anemia 1
HP:0001892 Abnormal bleeding 1
HP:0001903 Anemia 1
HP:0001907 Thromboembolism 1
HP:0002018 Nausea 1
HP:0002027 Abdominal pain 1
HP:0002040 Esophageal varix 1
HP:0002041 Intractable diarrhea 1
HP:0002094 Dyspnea 1
HP:0002105 Hemoptysis 1
HP:0002108 Spontaneous pneumothorax 1
HP:0002138 Subarachnoid hemorrhage 1
HP:0002204 Pulmonary embolism 1
HP:0002239 Gastrointestinal hemorrhage 1
HP:0002248 Hematemesis 1
HP:0002249 Melena 1
HP:0002317 Unsteady gait 1
HP:0002326 Transient ischemic attack 1
HP:0002488 Acute leukemia 1
HP:0002563 Constrictive pericarditis 1
HP:0002576 Intussusception 1
HP:0002583 Colitis 1
HP:0002595 Ileus 1
HP:0002617 Dilatation 1
HP:0002647 Aortic dissection 1
HP:0002664 Neoplasm 1
HP:0002716 Lymphadenopathy 1
HP:0002754 Osteomyelitis 1
HP:0002781 Upper airway obstruction 1
HP:0002816 Genu recurvatum 1
HP:0002860 Squamous cell carcinoma 1
HP:0002861 Melanoma 1
HP:0002862 Bladder carcinoma 1
HP:0003124 Hypercholesterolemia 1
HP:0003125 Reduced factor VIII activity 1
HP:0003418 Back pain 1
HP:0004936 Venous thrombosis 1
HP:0005110 Atrial fibrillation 1
HP:0005112 Abdominal aortic aneurysm 1
HP:0005374 Cellular immunodeficiency 1
HP:0006725 Pancreatic adenocarcinoma 1
HP:0009792 Teratoma 1
HP:0010550 Paraplegia 1
HP:0010628 Facial palsy 1
HP:0011029 Internal hemorrhage 1
HP:0011106 Hypovolemia 1
HP:0011506 Choroidal neovascularization 1
HP:0011900 Hypofibrinogenemia 1
HP:0011974 Myelofibrosis 1
HP:0012151 Hemothorax 1
HP:0012224 Circulating immune complexes 1
HP:0012418 Hypoxemia 1
HP:0012587 Macroscopic hematuria 1
HP:0012819 Myocarditis 1
HP:0012886 Hemorrhagic ovarian cyst 1
HP:0025343 Lupus anticoagulant 1
HP:0025615 Abscess 1
HP:0030433 Osteoid osteoma 1
HP:0031246 Nonproductive cough 1
HP:0031364 Ecchymosis 1
HP:0032118 Retinitis 1
HP:0032252 Granuloma 1
HP:0100021 Cerebral palsy 1
HP:0100026 Arteriovenous malformation 1
HP:0100309 Subdural hemorrhage 1
HP:0100310 Epidural hemorrhage 1
HP:0100584 Endocarditis 1
HP:0100769 Synovitis 1
HP:0100786 Hypersomnia 1
HP:0200043 Verrucae 1
HP:0200119 Acute hepatitis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID