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Results 1 - 10 of 33 for Factor V deficiency
  1. Factor V deficiency 
    Factor V deficiency is a rare bleeding disorder. The signs and symptoms of this condition can begin at any ... the most severe cases are apparent in childhood. Factor V deficiency commonly causes nosebleeds; easy bruising; bleeding under the ...
    https://medlineplus.gov/genetics/condition/factor-v-deficiency - Genetics
  2. Factor XIII deficiency 
    ... 10.1097/MOH.0b013e3283497e3e. Citation on PubMed Schroeder V, Kohler HP. Factor XIII deficiency: an update. Semin Thromb Hemost. 2013 Sep;39( ...
    https://medlineplus.gov/genetics/condition/factor-xiii-deficiency - Genetics
  3. Complement factor I deficiency 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov COMPLEMENT FACTOR I DEFICIENCY; CFID PubMed Baracho GV, Nudelman V, Isaac L. Molecular characterization of homozygous hereditary factor ...
    https://medlineplus.gov/.../condition/complement-factor-i-deficiency - Genetics
  4. Warfarin resistance 
    ... Citation on PubMed Rost S, Fregin A, Ivaskevicius V, Conzelmann E, Hortnagel K, Pelz HJ, Lappegard K, Seifried E, Scharrer I, Tuddenham EG, Muller CR, Strom TM, Oldenburg J. Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2. Nature. 2004 Feb 5;427(6974): ...
    https://medlineplus.gov/genetics/condition/warfarin-resistance - Genetics
  5. Von Willebrand disease 
    ... Vascular pseudohemophilia Von Willebrand disorder Von Willebrand's factor deficiency Genetic Testing Registry: von Willebrand disorder Von Willebrand ...
    https://medlineplus.gov/genetics/condition/von-willebrand-disease - Genetics
  6. Bernard-Soulier syndrome 
    ... Soulier type Platelet glycoprotein Ib deficiency Von Willebrand factor receptor deficiency Genetic Testing Registry: Bernard Soulier syndrome Bernard-Soulier ...
    https://medlineplus.gov/genetics/condition/bernard-soulier-syndrome - Genetics
  7. C3 glomerulopathy 
    ... Disease / Membranoproliferative Glomerulonephritis Type II Genetic Testing Registry: Factor H deficiency Genetic Testing Registry: Mesangiocapillary glomerulonephritis, type II Dense ...
    https://medlineplus.gov/genetics/condition/c3-glomerulopathy - Genetics
  8. Laron syndrome 
    ... W, Losekoot M. Spectrum of insulin-like growth factor deficiency. Endocr Dev. 2012;23:30-41. doi: 10. ...
    https://medlineplus.gov/genetics/condition/laron-syndrome - Genetics
  9. Alpha-1 antitrypsin deficiency 
    ... abstract available. Citation on PubMed Stoller JK, Hupertz V, Aboussouan LS. Alpha-1 Antitrypsin Deficiency. 2006 Oct 27 [updated 2023 Jun 1]. In: ...
    https://medlineplus.gov/.../condition/alpha-1-antitrypsin-deficiency - Genetics
  10. ACAD9 deficiency 
    ... LG, Houten SM. ACAD9, a complex I assembly factor with a moonlighting function in fatty acid oxidation deficiencies. Hum Mol Genet. 2014 Mar 1;23(5): ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
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