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Results 1 - 10 of 92 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. F5 gene 
    ... found to cause a rare bleeding disorder called factor V deficiency. These variants prevent the production of functional coagulation ... episodes of abnormal bleeding that can be severe. Factor V deficiency results from variants in both copies of the ...
    https://medlineplus.gov/genetics/gene/f5 - Genetics
  3. 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
  4. F13B gene 
    ... 1152/physrev.00016.2010. Citation on PubMed Schroeder V, Kohler HP. Factor XIII deficiency: an update. Semin Thromb Hemost. 2013 Sep;39( ...
    https://medlineplus.gov/genetics/gene/f13b - Genetics
  5. F13A1 gene 
    ... 1152/physrev.00016.2010. Citation on PubMed Schroeder V, Kohler HP. Factor XIII deficiency: an update. Semin Thromb Hemost. 2013 Sep;39( ...
    https://medlineplus.gov/genetics/gene/f13a1 - Genetics
  6. 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
  7. SUMF1 gene 
    ... 1 UNQ3037 Tests of SUMF1 PubMed SULFATASE-MODIFYING FACTOR 1; SUMF1 NCBI Gene ClinVar Annunziata I, Bouche V, Lombardi A, Settembre C, Ballabio A. Multiple sulfatase deficiency is due to hypomorphic mutations of the SUMF1 ...
    https://medlineplus.gov/genetics/gene/sumf1 - Genetics
  8. CFI gene 
    ... I; CFI NCBI Gene ClinVar Baracho GV, Nudelman V, Isaac L. Molecular characterization of homozygous hereditary factor I deficiency. Clin Exp Immunol. 2003 Feb;131(2):280- ...
    https://medlineplus.gov/genetics/gene/cfi - Genetics
  9. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... Glucose-6-phosphate dehydrogenase deficiency , also called G6PD deficiency Hereditary hemochromatosis Transthyretin amyloidosis Hereditary thrombophilia: prothrombin thrombophilia and factor V Leiden thrombophilia Alzheimer's disease Parkinson's disease ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  10. PROC gene 
    ... called factor V.) APC then works with factor V to inactivate factor VIIIa. At least 270 mutations in the PROC gene have been found to cause protein C deficiency. Most of these mutations change single protein building ...
    https://medlineplus.gov/genetics/gene/proc - Genetics
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