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Results 51 - 60 of 363 for Brain disorder
  1. BDNF gene 
    ... R, Fitches A. Evidence of associations between bipolar disorder and the brain-derived neurotrophic factor (BDNF) gene. Bipolar Disord. 2011 ...
    https://medlineplus.gov/genetics/gene/bdnf - Genetics
  2. ASPA gene 
    ... cause Canavan disease, which is a rare inherited disorder that affects brain development. Researchers have described two major forms of ...
    https://medlineplus.gov/genetics/gene/aspa - Genetics
  3. TREX1 gene 
    ... identified in people with Aicardi-Goutières syndrome, a disorder that involves severe brain dysfunction (encephalopathy), skin lesions, and other health problems. ...
    https://medlineplus.gov/genetics/gene/trex1 - Genetics
  4. SHANK3 gene 
    ... S, Waga C. SHANK3 as an autism spectrum disorder-associated gene. Brain Dev. 2013 Feb;35(2):106-10. doi: ...
    https://medlineplus.gov/genetics/gene/shank3 - Genetics
  5. ANKRD11 gene 
    ... facial features and intellectual disability. Many also have brain abnormalities and features of autism spectrum disorders, which are characterized by impaired communication and socialization ...
    https://medlineplus.gov/genetics/gene/ankrd11 - Genetics
  6. SUOX gene 
    ... with isolated sulfite oxidase deficiency (ISOD), a severe disorder that causes brain damage and is generally fatal in the first ...
    https://medlineplus.gov/genetics/gene/suox - Genetics
  7. CLPB gene 
    ... RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am J Hum Genet. 2015 Feb 5;96( ...
    https://medlineplus.gov/genetics/gene/clpb - Genetics
  8. SUCLA2 gene 
    ... 130(Pt 3):853-61. doi: 10.1093/brain/awl383. Epub 2007 Feb 7. Citation on PubMed Ostergaard E. Disorders caused by deficiency of succinate-CoA ligase. J ...
    https://medlineplus.gov/genetics/gene/sucla2 - Genetics
  9. SLC19A3 gene 
    ... with biotin-thiamine-responsive basal ganglia disease, a disorder that involves recurrent episodes of brain dysfunction (encephalopathy) and a variety of neurological problems ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  10. POLG gene 
    ... the POLG gene. MCHS is a POLG-related disorder that affects the muscles (myo-), brain (cerebro-), and liver (hepato-).Many variants in the ... decreasing mtDNA replication.As in other POLG-related disorders, people ... brain, or liver tissue. MtDNA depletion impairs oxidative phosphorylation ...
    https://medlineplus.gov/genetics/gene/polg - Genetics
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