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Results 1 - 10 of 86 for Hereditary disease
  1. ABCA1 gene 
    ... subfamily--gene and protein structures, functions and associated hereditary diseases. Pflugers Arch. 2007 Feb;453(5):581-9. ...
    https://medlineplus.gov/genetics/gene/abca1 - Genetics
  2. PLCG2 gene 
    ... activation of phospholipase C-gamma2 in the human hereditary disease PLAID. Cell Signal. 2016 Sep;28(9):1237- ...
    https://medlineplus.gov/genetics/gene/plcg2 - Genetics
  3. NLRP3 gene 
    ... M, Ozdogan H. Molecular and genetic characteristics of hereditary autoinflammatory diseases. Curr Drug Targets Inflamm Allergy. 2005 Feb;4( ...
    https://medlineplus.gov/genetics/gene/nlrp3 - Genetics
  4. FAH gene 
    ... correlates with clinical severity in a genetic liver disease, hereditary tyrosinemia. Hum Pathol. 2003 Dec;34(12):1313- ...
    https://medlineplus.gov/genetics/gene/fah - Genetics
  5. FH gene 
    ... Pinto PA, Neckers L, Linehan WM. Mechanisms of disease: hereditary leiomyomatosis and renal cell cancer--a distinct form ...
    https://medlineplus.gov/genetics/gene/fh - Genetics
  6. SLC40A1 gene 
    ... the SLC40A1 gene that cause a form of hereditary hemochromatosis called ferroportin disease, which is also sometimes referred to as type 4 hemochromatosis. This form of the disorder usually begins during adulthood. Hereditary hemochromatosis is a disorder that causes the body ...
    https://medlineplus.gov/genetics/gene/slc40a1 - Genetics
  7. MT-ND4L gene 
    ... K, Kisiel B, Piechota J, Bartnik E. Leber hereditary optic neuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology. J Appl Genet. 2003;44(4):529-38. Citation on PubMed Yu-Wai-Man P, Chinnery PF. Leber Hereditary Optic Neuropathy. 2000 Oct 26 [updated 2021 Mar ...
    https://medlineplus.gov/genetics/gene/mt-nd4l - Genetics
  8. HSPB1 gene 
    ... IP, Nicholson GA. Molecular genetics and mechanisms of disease in distal hereditary motor neuropathies: insights directing future genetic studies. Curr ...
    https://medlineplus.gov/genetics/gene/hspb1 - Genetics
  9. HAMP gene 
    ... Hepcidin: a putative iron-regulatory hormone relevant to hereditary hemochromatosis and the anemia of chronic disease. Proc Natl Acad Sci U S A. 2001 ...
    https://medlineplus.gov/genetics/gene/hamp - Genetics
  10. PINK1 gene 
    ... Harvey RJ, Dallapiccola B, Auburger G, Wood NW. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science. 2004 May ...
    https://medlineplus.gov/genetics/gene/pink1 - Genetics
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