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Results 1 - 10 of 191 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. CFH gene 
    ... nonfunctional version of the protein. The resulting shortage (deficiency) of complement factor H overactivates the complement system, which damages structures called ...
    https://medlineplus.gov/genetics/gene/cfh - Genetics
  3. Travelers' Health: Meningococcal Disease (Centers for Disease Control and Prevention)  
    Meningitis/Related Issues ... Meningitis ... Meningococcal Disease/Related Issues ... Meningococcal Disease ... Centers for Disease Control and Prevention ... Information about ...
    https://wwwnc.cdc.gov/.../infections-diseases/meningococcal-disease - External Health Links
  4. GFM1 gene 
    ... factor G1 Tests of GFM1 PubMed MITOCHONDRIAL ELONGATION FACTOR G1; GFM1 NCBI Gene ClinVar Antonicka H, Sasarman F, Kennaway NG, Shoubridge EA. The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation ...
    https://medlineplus.gov/genetics/gene/gfm1 - Genetics
  5. 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
  6. F10 gene 
    ... 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/gene/f10 - Genetics
  7. 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
  8. F7 gene 
    ... 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/gene/f7 - Genetics
  9. 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
  10. 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
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