| Rank (Similarity) |
PMID (PMCID) |
|
|---|---|---|
| 21 (22.1%) |
30127177 (6113844) |
Bilateral hemorrhagic proptosis due to an uncommon cause in ocular emergency. Pujari A, Mukhija R, Shashni A, Obedulla H, Meel R, Bajaj MS. Indian J Ophthalmol. 2018;66(9):1370-1371. |
| Proptosis Intracranial hemorrhage | ||
| Exophthalmos Hematoma Homo sapiens Male Visual Acuity X-Ray Computed Tomography Young Adult | ||
| 21 (22.1%) |
25811452 |
Successful treatment of immune tolerance induction with rituximab in a patient with severe hemophilia B and inhibitor. Kobayashi R, Sano H, Suzuki D, Kishimoto K, Yasuda K, Honjo R, Hirose M, Fujita S, Abe S, Kobayashi K. Blood Coagul Fibrinolysis. 2015;26(5):580-2. |
| Intracranial hemorrhage | ||
| F9 | ||
| Antineoplastic Agents Hemophilia B Homo sapiens Immune Tolerance Infant Male | ||
| 21 (22.1%) |
18756646 |
Head trauma and hemophilia B: case report about a challenging hematologic emergency. Falcon-Chevere JL, Cabanas JG. Bol Asoc Med P R. 2007;99(4):318-22. |
| Intracranial hemorrhage | ||
| F9 | ||
| Craniocerebral Trauma Hemophilia B Homo sapiens Intracranial Hemorrhage Male | ||
| 21 (22.1%) |
10608331 |
Spontaneous intracranial hemorrhage as the presenting sign of hemophilia B in a 3-month-old infant. Gerlacher GR. Pediatr Emerg Care. 1999;15(6):416-8. |
| Intracranial hemorrhage | ||
| Age Factors Age of Onset Hemophilia B Homo sapiens Infant Intracranial Hemorrhage Male | ||
| 21 (22.1%) |
3052146 |
Neonatal hemophilia B with intracranial hemorrhage. Case report. Ohga S, Kajiwara M, Toubo Y, Takeuchi T, Ohtsuka M, Sano Y, Ishii E, Ueda K. Am J Pediatr Hematol Oncol. 1988;10(3):244-8. |
| Intracranial hemorrhage | ||
| Cerebral Hemorrhage Hematoma, Subdural Hemophilia B Homo sapiens Infant, Newborn Male | ||
| 21 (22.1%) |
643159 |
[Surgical treatment of intracranial hematoma in an infant with hemophilia B (author's transl)]. Tomono Y, Nakada Y. No Shinkei Geka. 1978;6(3):281-6. |
| Hydrocephalus Intracranial hemorrhage | ||
| Blood Transfusion Cerebral Hemorrhage Hematoma Hemophilia B Homo sapiens Infant Male | ||
| 27 (20.5%) |
10517121 |
[A patient with isolated prolongation of aPTT without hemorrhagic diathesis anamnesis: severe, hereditary factor XII deficiency]. Zeerleder S, Asmis L, Redondo M, Sulzer I, Lammle B. Ther Umsch. 1999;56(9):509-12. |
| Venous thrombosis Lupus anticoagulant | ||
| F8 F9 | ||
| Adult Differential Diagnosis Factor XII Deficiency Females Hemorrhagic Disorders Homo sapiens | ||
| 27 (20.5%) |
6265056 |
Acquired dysfibrinogenemia in a hemophiliac with hepatoma: resolution of fibrinogen dysfunction following chemotherapy. Ballard JO, Kelly GA, Kukrika MD, Sanders JC, Eyster ME. Cancer. 1981;48(3):686-90. |
| Dysfibrinogenemia Sepsis | ||
| FGB | ||
| Antineoplastic Agents Blood Coagulation Disorders Hemophilia A Hemophilia B Homo sapiens Male Neoplasm Metastasis | ||
| 27 (20.5%) |
3778094 |
[Acquired immunodeficiency syndrome in an adolescent hemophiliac]. Pichot F, Bader B, Laurian Y, Alvin P, Tardieu M, Tchernia G, Larrieu MJ, Courtecuisse V. Arch Fr Pediatr. 1986;43(5):341-4. |
| Lymphopenia | ||
| Acquired Immunodeficiency Syndrome Brain Diseases Hemophilia B Homo sapiens Male Opportunistic Infections Toxoplasmosis | ||
| 27 (20.5%) |
1324748 |
Herpes simplex virus type 1 and human immunodeficiency virus type 1 antigens in platelets from a hemophilia B patient with human immunodeficiency virus type 1-related thrombocytopenia. Koike K, Matsumoto K, Arai M, Yorifuji H, Fukutake K, Fujimaki M. Int J Hematol. 1992;55(2):205-10. |
| Thrombocytopenia Immunodeficiency | ||
| Adult Antigens, Viral Blood Platelets HIV Antigens HIV Infections HIV-1 Hemophilia A Homo sapiens Human Platelet Antigens Immune Complex Diseases Male Molecular Weight Simplexvirus Thrombocytopenia |
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%) |
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 |
Total: 0
| Gene Symbol | Gene Name | Entrez Gene ID |
|---|