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Results 1 - 10 of 19 for Congenital factor V deficiency
  1. Factor V deficiency 
    ... s disease Parahemophilia Proaccelerin deficiency Genetic Testing Registry: Congenital factor V deficiency Congenital factor V deficiency National Organization for Rare ...
    https://medlineplus.gov/genetics/condition/factor-v-deficiency - Genetics
  2. Factor XIII deficiency 
    ... Testing Registry: Factor XIII, A subunit, deficiency of Congenital factor XIII deficiency ... Biswas A, Ivaskevicius V, Thomas A, Oldenburg J. Coagulation factor XIII deficiency. ...
    https://medlineplus.gov/genetics/condition/factor-xiii-deficiency - Genetics
  3. Congenital leptin deficiency 
    ... be altered in congenital leptin deficiency are unknown.Congenital leptin deficiency is a rare cause of obesity. Researchers are studying the factors involved in more common forms of obesity. LEP ...
    https://medlineplus.gov/.../condition/congenital-leptin-deficiency - Genetics
  4. 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
  5. LEP gene 
    ... involvement and how it may be altered in congenital leptin deficiency are unknown. More About This Health Condition LEP_HUMAN LEPD leptin (murine obesity homolog) leptin (obesity homolog, mouse) OB obese protein obese, mouse, homolog of obesity factor OBS Tests of LEP PubMed LEPTIN; LEP NCBI ...
    https://medlineplus.gov/genetics/gene/lep - Genetics
  6. Prothrombin thrombophilia 
    ... 000. Hyperprothrombinemia Prothrombin G20210A Thrombophilia ... PubMed Bosler D, Mattson J, Crisan ...
    https://medlineplus.gov/genetics/condition/prothrombin-thrombophilia - Genetics
  7. 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
  8. FH gene 
    ... 00470.x. Citation on PubMed Bayley JP, Launonen V, Tomlinson IP. The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency. BMC Med Genet. 2008 Mar 25;9:20. ...
    https://medlineplus.gov/genetics/gene/fh - Genetics
  9. X-linked sideroblastic anemia 
    ... 10.1007/BF02110031. Citation on PubMed Bottomley SS. Congenital ... as a predisposing factor for late-onset X-linked sideroblastic anemia in ...
    https://medlineplus.gov/.../condition/x-linked-sideroblastic-anemia - Genetics
  10. COG5-congenital disorder of glycosylation 
    ... Kleinert P, Schnabel S, Baumgartner M, Hennet T. Deficiency in COG5 causes a ... Rymen D, Keldermans L, Race V, Regal L, Deconinck N, Dionisi-Vici C, Fung ...
    https://medlineplus.gov/...cog5-congenital-disorder-of-glycosylation - Genetics
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