Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 34 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 age, although the most severe cases are apparent ...
    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. Prothrombin thrombophilia 
    ... second most common inherited form of thrombophilia after factor V Leiden thrombophilia. Approximately 1 in 50 people in ... Richards CS. Technical standards and guidelines: venous thromboembolism (Factor V Leiden and prothrombin 20210G >A testing): a disease- ...
    https://medlineplus.gov/genetics/condition/prothrombin-thrombophilia - Genetics
  8. 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
  9. 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
  10. 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
previous · 1 · 2 · 3 · 4 · next