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Results 1 - 10 of 36 for Allele
  1. Huntington's disease 
    Huntington's disease is a progressive brain disorder that causes uncontrolled movements, emotional problems, and loss of thinking ability (cognition).Adult-onset ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease - Genetics
  2. Alpha thalassemia 
    ... in each cell. Each copy is called an allele. For each gene, one allele is inherited from a person's father, and ... s mother. As a result, there are four alleles that produce alpha-globin. The different types of ...
    https://medlineplus.gov/genetics/condition/alpha-thalassemia - Genetics
  3. Alpha-1 antitrypsin deficiency 
    ... to the genetic trait.The most common version (allele) of the SERPINA1 gene, called M, produces normal ... general population have two copies of the M allele (MM) in each cell. Other versions of the ...
    https://medlineplus.gov/.../condition/alpha-1-antitrypsin-deficiency - Genetics
  4. Alzheimer's disease 
    ... a variant of this gene called the e4 allele seems to increase an individual's risk for ... who inherit one copy of the APOE e4 allele have an increased chance of developing the disease; ...
    https://medlineplus.gov/genetics/condition/alzheimers-disease - Genetics
  5. Dementia with Lewy bodies 
    ... the APOE gene, one version, called the e4 allele, seems to increase an individual's risk for ... that the apolipoprotein E produced from the e4 allele of the APOE gene may disrupt the transport ...
    https://medlineplus.gov/genetics/condition/dementia-with-lewy-bodies - Genetics
  6. Warfarin sensitivity 
    ... Working Group on Pharmacogenetic Testing of CYP2C9, VKORC1 Alleles for Warfarin Use. Pharmacogenetic testing of CYP2C9 and VKORC1 alleles for warfarin. Genet Med. 2008 Feb;10(2): ...
    https://medlineplus.gov/genetics/condition/warfarin-sensitivity - Genetics
  7. Crigler-Najjar syndrome 
    ... Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation. Hum Mutat. 2005 Mar; ... in The Netherlands: identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 ...
    https://medlineplus.gov/genetics/condition/crigler-najjar-syndrome - Genetics
  8. Autoimmune Addison disease 
    ... Rewers MJ, Eisenbarth GS. DRB1*04 and DQ alleles: expression of 21-hydroxylase autoantibodies and risk of ...
    https://medlineplus.gov/.../condition/autoimmune-addison-disease - Genetics
  9. Robinow syndrome 
    ... VR, Lupski JR, Brunner HG, Carvalho CMB. DVL3 Alleles Resulting in a -1 Frameshift of the Last ...
    https://medlineplus.gov/genetics/condition/robinow-syndrome - Genetics
  10. Metachromatic leukodystrophy 
    ... identification and functional characterization of 11 novel ARSA alleles. Hum Mutat. 2008 Nov;29(11):E220-30. ...
    https://medlineplus.gov/.../condition/metachromatic-leukodystrophy - Genetics
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