Hemophilia B

Hemophilia B is a form of hemophilia (see this term) characterized by spontaneous or prolonged hemorrhages due to factor IX deficiency.



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Narrow down the case reports



Total: 116 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
95
(5.0%)
2474882
Management of urinary retention due to benign prostatic hyperplasia using luteinizing hormone-releasing hormone agonist.
Schlegel PN, Brendler CB.
Urology. 1989;34(2):69-72.
Urinary retention
GNRH1
Aged, 80 and over Drug Evaluation Hemophilia B Homo sapiens Male Middle Aged Organ Size Prostate Prostatic Hyperplasia Ultrasonography Urination Disorders
95
(5.0%)
2314403
[Intraspinal, extradural hemorrhage in a 7-year-old boy with hemophilia B].
Jost W, Graf N, Pindur G, Sitzmann FC.
Monatsschr Kinderheilkd. 1990;138(1):36-7.
Spinal cord compression
Child Follow-Up Studies HIV Seropositivity HIV-1 Hematoma, Epidural, Cranial Hemophilia B Homo sapiens Male Spinal Diseases X-Ray Computed Tomography
95
(5.0%)
2120893
Group B streptococcal polyarthritis complicating hemophilia B.
Hartmann LC, Nauseef WM.
Acta Haematol. 1990;84(2):95-7.
Septic arthritis
Alcoholic Intoxication, Chronic Arthritis, Infectious Hemophilia B Homo sapiens Male Middle Aged Streptococcal Infections Streptococcus agalactiae
95
(5.0%)
1530122
Intraspinal hematomas in hemophilia.
Hamre MR, Haller JS.
Am J Pediatr Hematol Oncol. 1992;14(2):166-9.
Urinary retention
Child Hematoma Hemophilia A Hemophilia B Homo sapiens Male Spinal Diseases
95
(5.0%)
1514211
[ESWL in hemophilia B].
Schlick R, Djamilian M, de Riese W, Truss M, Allhoff EP, Jonas U.
Urologe A. 1992;31(4):238-42.
Nephrolithiasis
Adult Hemophilia B Homo sapiens Kidney Calculi Lithotripsy Male Premedication
95
(5.0%)
515803
Coagulopathy in nephrotic syndrome at the time of renal biopsy.
Tanphaichitr P, Loharjun C, Isarangkura P, Hathirat P.
Southeast Asian J Trop Med Public Health. 1979;10(3):398-9.
Nephrotic syndrome
Biopsy Blood Coagulation Disorders Child Hematuria Hemophilia B Homo sapiens Kidney Male Nephrotic Syndrome
        

Phenotype(s) retrieved from Orphanet

    Total: 14

HPO ID Term Frequency
HP:0000790 Hematuria Very frequent (99-80%)
HP:0001058 Poor wound healing Very frequent (99-80%)
HP:0002170 Intracranial hemorrhage Very frequent (99-80%)
HP:0003010 Prolonged bleeding time Very frequent (99-80%)
HP:0003645 Prolonged partial thromboplastin time Very frequent (99-80%)
HP:0004406 Spontaneous, recurrent epistaxis Very frequent (99-80%)
HP:0004846 Prolonged bleeding after surgery Very frequent (99-80%)
HP:0005261 Joint hemorrhage Very frequent (99-80%)
HP:0006298 Prolonged bleeding after dental extraction Very frequent (99-80%)
HP:0011858 Reduced factor IX activity Very frequent (99-80%)
HP:0012233 Intramuscular hematoma Very frequent (99-80%)
HP:0012541 Cephalohematoma Very frequent (99-80%)
HP:0040232 Delayed onset bleeding Very frequent (99-80%)
HP:0400008 Menometrorrhagia Very frequent (99-80%)


Phenotype(s) retrieved from case reports

    Total: 51

HPO ID Term # of case reports
HP:0012115 Hepatitis 7
HP:0002721 Immunodeficiency 6
HP:0001394 Cirrhosis 4
HP:0002650 Scoliosis 3
HP:0031625 Pseudoaneurysm 3
HP:0000100 Nephrotic syndrome 2
HP:0000421 Epistaxis 2
HP:0001658 Myocardial infarction 2
HP:0002170 Intracranial hemorrhage 2
HP:0011886 Hyphema 2
HP:0012223 Splenic rupture 2
HP:0031273 Shock 2
HP:0000016 Urinary retention 1
HP:0000939 Osteoporosis 1
HP:0001249 Intellectual disability 1
HP:0001541 Ascites 1
HP:0001629 Ventricular septal defect 1
HP:0001681 Angina pectoris 1
HP:0001873 Thrombocytopenia 1
HP:0001888 Lymphopenia 1
HP:0001907 Thromboembolism 1
HP:0001927 Acanthocytosis 1
HP:0002014 Diarrhea 1
HP:0002040 Esophageal varix 1
HP:0002105 Hemoptysis 1
HP:0002107 Pneumothorax 1
HP:0002239 Gastrointestinal hemorrhage 1
HP:0002248 Hematemesis 1
HP:0002249 Melena 1
HP:0002621 Atherosclerosis 1
HP:0002664 Neoplasm 1
HP:0002671 Basal cell carcinoma 1
HP:0002835 Aspiration 1
HP:0002870 Obstructive sleep apnea 1
HP:0003040 Arthropathy 1
HP:0004326 Cachexia 1
HP:0004395 Malnutrition 1
HP:0007340 Lower limb muscle weakness 1
HP:0009797 Cholesteatoma 1
HP:0009830 Peripheral neuropathy 1
HP:0011851 Hemopericardium 1
HP:0012151 Hemothorax 1
HP:0012315 Histiocytoma 1
HP:0012393 Allergy 1
HP:0012636 Retinal vein occlusion 1
HP:0012740 Papilloma 1
HP:0025615 Abscess 1
HP:0032118 Retinitis 1
HP:0040223 Pulmonary hemorrhage 1
HP:0100762 Hemobilia 1
HP:0200123 Chronic hepatitis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID