| Rank (Similarity) |
PMID (PMCID) |
|
|---|---|---|
| 9 (26.6%) |
8366581 |
[A giant esophageal ulcer in a hemophiliac with HIV infection]. Muraoka K, Hara T, Kajiwara T, Simoda Y, Miyamoto Y, Miyazaki S. Rinsho Ketsueki. 1993;34(6):759-63. |
| Hematemesis | ||
| Administration, Oral Adult Combination Drug Therapy Esophageal Diseases HIV Infections Hemophilia B Homo sapiens Male Ulcer | ||
| 9 (26.6%) |
8048983 |
Hemophilia B in a neonate: unusual early spontaneous gastrointestinal bleeding. Reish O, Nachum E, Naor N, Ghoshen J, Merlob P. Am J Perinatol. 1994;11(3):192-3. |
| Melena | ||
| Gastrointestinal Hemorrhage Hemophilia B Homo sapiens Infant, Newborn Male | ||
| 9 (26.6%) |
6971362 |
Gastrectomy in siblings with Christmas disease (hemophilia B). Mizumoto R, Kawarada Y, Ogura Y. Jpn J Surg. 1980;10(4):328-37. |
| Gastrointestinal hemorrhage | ||
| Blood Transfusion Gastrectomy Gastrointestinal Hemorrhage Hemophilia B Homo sapiens Male Middle Aged Stomach Neoplasms | ||
| 14 (26.5%) |
31106079 |
First Case of Acquired Hemophilia B in a Patient with HIV Infection: Case Report and Literature Review. Paramo L, Enciso Olivera LJ, Norena I, Amaya MA, Santacruz JC. Cureus. 2019;11(3):e4179. |
| Diarrhea Hepatitis Bacteremia | ||
| 15 (25.2%) |
7301394 |
[Biphasic splenic rupture in a hemophilic child (author's transl)]. Kaulfersch W, Hollwarth M, Muntean W. Padiatr Padol. 1981;16(4):465-7. |
| Splenic rupture | ||
| Child Hemophilia B Homo sapiens Male Nonpenetrating Wounds Splenic Rupture | ||
| 16 (25.0%) |
16999730 |
Delayed diagnosis of congenital factor IX deficiency (Christmas disease) in a girl with Turner's Syndrome. Kelsey G, Monagle P, Barnes C. Clin Lab Haematol. 2006;28(5):355-6. |
| Intrahepatic cholestasis | ||
| Anemia Child Cholestasis Differential Diagnosis Females Hemophilia B Homo sapiens Time Factors Turner Syndrome | ||
| 17 (23.0%) |
25213132 |
Living donor liver transplantation from an asymptomatic donor with mild coagulation factor IX deficiency: report of a case. Sanada Y, Sasanuma H, Sakuma Y, Morishima K, Kasahara N, Kaneda Y, Miki A, Fujiwara T, Shimizu A, Hyodo M, Hirata Y, Yamada N, Okada N, Ihara Y, Urahashi T, Madoiwa S, Mimuro J, Mizuta K, Yasuda Y. Pediatr Transplant. 2014;18(8):E270-3. |
| Biliary atresia | ||
| CORO7 F9 | ||
| Adult Asymptomatic Diseases Biliary Atresia Females Hemophilia B Homo sapiens Infant Living Donors | ||
| 17 (23.0%) |
18636674 |
Hemobilia as the initial manifestation of cholangiocarcinoma in a hemophilia B patient. Manolakis AC, Kapsoritakis AN, Tsikouras AD, Tsiopoulos FD, Psychos AK, Potamianos SP. World J Gastroenterol. 2008;14(26):4241-4. |
| Hemobilia | ||
| Bile Duct Neoplasms Biliary Tract Hemorrhage CA-19-9 Antigen Cholangiocarcinoma Cholangiopancreatography, Magnetic Resonance Endoscopic Retrograde Cholangiopancreatography Hemophilia B Homo sapiens Male | ||
| 19 (22.5%) |
25515020 (4279815) |
Renal thromboembolism during treatment with recombinant activated factor VII (rFVIIa) in a child with hemophilia B with factor IX inhibitors. Miloevic D, Bilic E, Batinic D, Poropat M, tern-Padovan R, Galic S, Turudic D. BMC Pediatr. 2014;14:315. |
| Hematuria Thromboembolism | ||
| F9 | ||
| Blood Coagulation Factor Inhibitors Child Hematuria Hemophilia B Homo sapiens Kidney Male Recombinant Proteins Thromboembolism | ||
| 20 (22.5%) |
8810766 |
[Sulfamethoxazole-trimethoprim-induced pneumonitis in a patient with hemophilia B who was infected with the human immunodeficiency virus]. Yamagishi T, Yoshida S, Fukutake K, Utsumi K, Ichinose Y. Nihon Kyobu Shikkan Gakkai Zasshi. 1996;34(7):822-8. |
| Skin rash Fever | ||
| AIDS-Related Opportunistic Infections Acquired Immunodeficiency Syndrome Adult Anti-Bacterial Agents Combination Drug Therapy Differential Diagnosis Hemophilia B Homo sapiens Immunocompromised Host Lung Diseases, Interstitial Male Trimethoprim-Sulfamethoxazole Combination |
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 |
|---|