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Results 1 - 10 of 45 for Factor H deficiency
  1. 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
  2. Factor X deficiency 
    ... Auerswald G, Ruiz-Saez A, Navarrete M, Pollmann H, Lopaciuk S, Batorova A, Wulff K; Greifswald Factor X Deficiency Study Group. Factor X deficiency: clinical manifestation of ...
    https://medlineplus.gov/genetics/condition/factor-x-deficiency - Genetics
  3. Factor VII deficiency 
    ... S, Astermark J, Batorova A, Kreuz W, Pollmann H, Ruiz-Saez A, De Bosch N, Salazar-Sanchez L; Greifswald Factor FVII Deficiency Study Group. Factor VII deficiency: clinical manifestation of ...
    https://medlineplus.gov/genetics/condition/factor-vii-deficiency - Genetics
  4. Combined oxidative phosphorylation deficiency 1 
    ... PM, Weraarpachai W, Haller W, Schreurs M, Venselaar H, Rodenburg RJ, Smeitink JA, van den Heuvel LP. Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle. Eur J ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  5. ACAD9 deficiency 
    ... 002. Citation on PubMed Nouws J, Te Brinke H, Nijtmans 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
  6. Complement factor I deficiency 
    ... N, Miteva MA, Genel F, Zelazko M, Marquart H, Muller K, Sjoholm AG, Truedsson L, Villoutreix BO, Blom AM. Genetic, molecular and functional analyses of complement factor I deficiency. Eur J Immunol. 2009 Jan;39(1):310- ...
    https://medlineplus.gov/.../condition/complement-factor-i-deficiency - Genetics
  7. COG5-congenital disorder of glycosylation 
    ... COG) complex and the golgin TATA element modulatory factor (TMF). J Biol Chem. 2013 Feb ... M, Hennet T. Deficiency in COG5 causes a moderate form of congenital ...
    https://medlineplus.gov/...cog5-congenital-disorder-of-glycosylation - Genetics
  8. Prekallikrein deficiency 
    ... symptoms of the condition. Congenital prekallikrein deficiency Fletcher factor deficiency Fletcher trait PKK deficiency Genetic Testing Registry: Prekallikrein ...
    https://medlineplus.gov/genetics/condition/prekallikrein-deficiency - Genetics
  9. 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
  10. Warfarin resistance 
    ... 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
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