*  Factor VIII
GeneReviews/NCBI/NIH/UW entry on Hemophilia A The Coagulation Factor VIII Protein Factor VIII at the US National Library of ... Gitschier J (1991). "The molecular basis of hemophilia A". Annals of the New York Academy of Sciences. 614 (1 Process in Va): ... Defects in this gene result in hemophilia A, a recessive X-linked coagulation disorder. Factor VIII is produced in liver ... Hemophilia A has been corrected by liver transplantation. Transplanting hepatocytes was ineffective, but liver endothelial ...
*  Haemophilia
There are several types of haemophilia: haemophilia A, haemophilia B, haemophilia C, parahaemophilia, and acquired haemophilia ... Haemophilia A affects about 1 in 5,000-10,000, while haemophilia B affects about 1 in 40,000, males at birth. As haemophilia A ... National Hemophilia Federation. Key facts: what is haemophilia? Archived 2009-05-23 at the Wayback Machine. The Haemophilia ... There are two main types of haemophilia: haemophilia A, which occurs due to not enough clotting factor VIII, and haemophilia B ...
*  Haemophilia in European royalty
Because the last known descendant of Queen Victoria with haemophilia died in the 1940s, the exact type of haemophilia found in ... ISBN 0-7509-1199-9. "Hemophilia: The Royal Disease" Family tree of Queen Victoria and her descendants Haemophilia in Queen ... Although an individual's haemophilia can usually be traced in the ancestry, in about 30% of cases there is no family history of ... Maurice's haemophilia is disputed by various sources: It seems unlikely that a known haemophiliac would be allowed to serve in ...
*  Haemophilia B
Russia and Spain as haemophilia B on the basis of genetic markers. Haemophilia C Haemophilia in European royalty "Hemophilia B ... It is the second-most common form of haemophilia, rarer than haemophilia A. Haemophilia B was first recognized as a different ... Haemophilia B (or hemophilia B) is a blood clotting disorder caused by a mutation of the factor IX gene, leading to a ... The presentation of hemophilia B is consistent with easy bruising, urinary tract bleed and nosebleeds. Additionally, the ...
*  Porphyric hemophilia
... may refer to: Porphyria, using an uncommon name for the conditions Vampirism, a term describing being a ...
*  Canadian Hemophilia Society
It is named for the blood disease hemophilia. World Federation of Hemophilia "Canadian Hemophilia Society Homepage". Hemophilia ... The Canadian Hemophilia Society (CHS) is a non-profit organization founded in 1953 whose mission is to lead the fight against ...
*  World Federation of Hemophilia
"World Hemophilia Day 2010". World Federation of Hemophilia. Retrieved 2010-04-17. "World Hemophilia Day 2009". World Federation ... World Hemophilia Day is an international observance held annually on April 17 by the WFH. It is an awareness day for hemophilia ... "World Hemophilia Day - 2008". Retrieved 2010-04-17. "World Hemophilia Day". Retrieved 2010-04-17. World Federation of ... "World Federation of Hemophilia". Retrieved 2012-08-16. "Media Advisory: World Hemophilia Day Tulip Sale Event, April 15, 2010 ...
*  Haemophilia C
... as common as haemophilia A. In terms of the signs/symptoms of haemophilia C, unlike individuals with Haemophilia A and B, ... However, people affected with haemophilia C might experience symptoms closely related to those of other forms of haemophilia ... Haemophilia C is caused by a deficiency of coagulation factor XI and is distinguished from haemophilia A and B by the fact it ... In terms of hemophilia C medication cyklokapron is often used for both treatment after an incident of bleeding and as a ...
*  Haemophilia A
... (or hemophilia A) is a genetic deficiency in clotting factor VIII, which causes increased bleeding and usually ... Individuals with more severe haemophilia suffer more severe and more frequent bleeding, while others with mild haemophilia ... Haemophilia leads to a severely increased risk of prolonged bleeding from common injuries, or in severe cases bleeding may be ... Factor VIII medication may be used to treat and prevent bleeding in people with haemophilia A. In terms of the symptoms of ...
*  Contaminated haemophilia blood products
... were a serious public health problem in the late 1970s up to 1985. These products ... The case followed complaints by families of some 170 people, many of them children, suffering from haemophilia and the blood ... met with leaders of the haemophilia community to outline the terms of a $125 million offer. Rejecting the offer, David Shrager ... "appear responsible for AIDS among haemophilia patients." By May 1983, a Cutter rival began making a heat-treated concentrate ...
*  United Kingdom Haemophilia Centre Doctors' Organisation
The United Kingdom Haemophilia Centre Doctors' Organisation before 1993 was known as the United Kingdom Haemophilia Centre ... this information is stored on the National Haemophilia Database which is managed and run by UKHCDO. "ukhcdo". ukhcdo.org. ...
*  DMOZ - Health: Conditions and Diseases: Blood Disorders: Hemophilia
There are two types of hemophilia: hemophilia A, or clotting factor VIII deficiency, and hemophilia B, or clotting factor IX ... About one third of hemophilia cases occur with no previous family history; this is called sporadic hemophilia. It is assumed ... Hemophilia is a genetically inherited bleeding disorder. There are two types of hemophilia: hemophilia A, or clotting factor ... Hemophilia Ontario Committed to improve the quality of life of people affected by hemophilia and related blood conditions. ...
*  DMOZ - Health: Conditions and Diseases: Blood Disorders: Hemophilia: Organizations
Haemophilia Foundation of New Zealand Inc. Aims to serve the needs of people with haemophilia and other related genetic ... UK Haemophilia Society Working to secure the best possible care, treatment and support for people with haemophilia, related ... Canadian Hemophilia Society Dedicated to improving the quality of life for persons with hemophilia and other inherited bleeding ... World Federation of Hemophilia A global network of healthcare providers, national hemophilia associations, people with ...
*  United Kingdom tainted blood scandal
"Hemophilia Facts". CDC. August 26, 2014. Retrieved 8 September 2016. "Gene therapy used to treat haemophilia". nhs.uk. ... Haemophilia is a mostly inherited genetic disorder that impairs the body's ability to clot, a process needed to stop bleeding. ... In 2015 Baxter split-off its haemophilia sector to create Baxalta. In 2016 Baxalta was acquired by Shire plc for $32bn. Immuno ... The tainted blood scandal in the United Kingdom arose after 3,891 people with Haemophilia became infected with hepatitis C and ...
*  Obligate carrier
Hemophilia, or haemophilia, is an X-linked recessive disorder that impairs the body's control over blood clotting. Haemophilia ... "Heredity of hemophilia". Canadian Hemophilia Society. Canadian Hemophilia Society. Retrieved 2015. Check date values in: , ... al (1993). "Haemophilia: strategies for carrier detection and prenatal diagnosis". Bull World Health Organ. 71 (3-4): 429-458. ... Check date values in: ,access-date= (help) "Carrier Diagnosis". World Federation of Hemophilia. Retrieved 2015. Check date ...
*  List of OMIM disorder codes
STX11 Hemophilia B; 306900; F9 Hemorrhagic diathesis due to \'antithrombin\' Pittsburgh; 613490; SERPINA1 Hemosiderosis, ...
*  Congenital afibrinogenemia
"Factor I deficiency (Fibrinogen deficiency) - Canadian Hemophilia Society". www.hemophilia.ca. Retrieved 2015-11-12. " ... Haemophilia. 22: e48-e51. doi:10.1111/hae.12802. ISSN 1365-2516. ...
*  M. K. Muneer
MCC-THAS-Hemophilia Society ,". Pedblood.org. Archived from the original on 27 July 2011. Retrieved 1 July 2011. ... He is a qualified medical doctor and patron of MCC-THAS-Haemophilia Society. He passed his MBBS from Government Medical College ...
*  Ortner's syndrome
Hermans C, Manocha S, McLaughlin JE, Lipman M, Lee CA (September 2005). "Ortner syndrome and haemophilia". Haemophilia. 11 (5 ...
*  Variant Creutzfeldt-Jakob disease
Ironside, JW (Jul 2010). "Variant Creutzfeldt-Jakob disease". Haemophilia. 16 Suppl 5: 175-80. doi:10.1111/j.1365-2516.2010. ...
*  Prion
Haemophilia. 12 Suppl 1: 8-15; discussion 26-8. doi:10.1111/j.1365-2516.2006.01195.x. PMID 16445812. Groschup MH, Kretzschmar ...
*  Factor V
Deficiency is associated with a rare mild form of hemophilia (termed parahemophilia or Owren parahemophilia), the incidence of ... Huang JN, Koerper MA (November 2008). "Factor V deficiency: a concise review". Haemophilia. 14 (6): 1164-9. doi:10.1111/j.1365- ...
*  Purpura fulminans
Goldenberg NA, Manco-Johnson MJ (2008). "Protein C deficiency". Haemophilia. 14 (6): 1214-1221. doi:10.1111/j.1365-2516.2008. ...
*  Von Willebrand disease
Hemophilia.org Haemophilia.org.uk WFH.org, World Federation of Hemophilia Ukhcdo.org UK Haemophilia Centre Directors ... National Hemophilia Federation. "Von Willebrand Disease". National Hemophilia Federation. Retrieved 3 December 2017. James P, ... National Hemophilia Federation. "Von Willebrand Disease". National Hemophilia Federation. Retrieved 3 December 2017. National ... 2004). "The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization". Haemophilia ...
*  Rob Horne (professor)
... haemophilia; depression; bipolar disorder; rheumatoid arthritis; inflammatory bowel disease and also for newly prescribed ...