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Results 1 - 10 of 34 for Thrombocytopenia 9
  1. MYH9 gene 
    ... most affected by a lack of functional myosin-9, accounting for the thrombocytopenia seen in all individuals with MYH9-related disorder. More About This Health Condition MedlinePlus Genetics provides ... MYH9_HUMAN myosin heavy chain, non-muscle IIa myosin, heavy chain 9, non-muscle myosin-9 NMHC-II-A NMMHC ...
    https://medlineplus.gov/genetics/gene/myh9 - Genetics
  2. Thrombocytopenia-absent radius syndrome 
    ... Citation on PubMed de Ybarrondo L, Barratt MS. Thrombocytopenia absent radius syndrome. Pediatr Rev. 2011 Sep;32(9):399-400; discussion 400. doi: 10.1542/pir. ...
    https://medlineplus.gov/.../thrombocytopenia-absent-radius-syndrome - Genetics
  3. ITGB3 gene 
    ... L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis. Br J Haematol. 2013 Feb;160(4):521-9. doi: 10.1111/bjh.12160. Epub 2012 Dec ...
    https://medlineplus.gov/genetics/gene/itgb3 - Genetics
  4. Dyserythropoietic anemia and thrombocytopenia 
    ... PD, Balamohan SM, Raskind WH, Kacena MA. Inherited thrombocytopenia due to GATA-1 mutations. Semin Thromb Hemost. 2011 Sep;37(6):682-9. doi: 10.1055/s-0031-1291378. Epub 2011 ...
    https://medlineplus.gov/...rythropoietic-anemia-and-thrombocytopenia - Genetics
  5. X chromosome 
    ... idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. J Med Genet. 1997 Aug;34(8):666-9. doi: 10.1136/jmg.34.8.666. Citation ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  6. Thrombotic thrombocytopenic purpura 
    ... reduced level of circulating platelets is known as thrombocytopenia. Thrombocytopenia can lead to small areas of bleeding just ... inherited. Chronic relapsing thrombotic thrombocytopenic purpura Familial ... thrombotic thrombocytopenic TTP Genetic ...
    https://medlineplus.gov/.../thrombotic-thrombocytopenic-purpura - Genetics
  7. Jacobsen syndrome 
    ... disorder 11q- deletion syndrome 11q23 deletion disorder Jacobsen thrombocytopenia Genetic Testing Registry: 11q partial monosomy syndrome Jacobsen ... Orphanet J Rare Dis. 2009 Mar 7;4:9. doi: 10.1186/1750-1172-4-9. Citation ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  8. Von Willebrand disease 
    ... J Thromb Haemost. 2007 Jun;5(6):1165-9. doi: 10.1111/j.1538-7836.2007.02563. ...
    https://medlineplus.gov/genetics/condition/von-willebrand-disease - Genetics
  9. X-linked thrombocytopenia 
    ... correlation. Blood. 2004 Dec 15;104(13):4010-9. doi: 10.1182/blood-2003-05-1592. ... of x-linked thrombocytopenia in the chinese with novel mutations. J Clin ...
    https://medlineplus.gov/genetics/condition/x-linked-thrombocytopenia - Genetics
  10. WAS gene 
    ... gene have been found to cause X-linked thrombocytopenia, a blood disorder characterized by a decrease in ... the actin cytoskeleton. In people with X-linked thrombocytopenia, these signaling problems primarily affect the development of ...
    https://medlineplus.gov/genetics/gene/was - Genetics
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