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Results 1 - 9 of 9 for codominant
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  1. If a genetic disorder runs in my family, what are the chances that my children will have the condition?: MedlinePlus ... 
    ... disorder will inherit the condition from their father. Codominant inheritance: In codominant inheritance , each parent contributes a different version of ...
    https://medlineplus.gov/.../understanding/inheritance/riskassessment - Genetics
  2. What are the different ways a genetic condition can be inherited?: MedlinePlus Genetics 
    ... Y chromosome infertility , some cases of Swyer syndrome Codominant In codominant inheritance , two different versions (alleles) of a gene ...
    https://medlineplus.gov/.../inheritance/inheritancepatterns - Genetics
  3. Learning about Alpha-1 Antitrypsin Deficiency (AATD) From the National Institutes of Health (National Human Genome Research Institute)  
    Alpha-1 Antitrypsin Deficiency/Start Here ... Alpha-1 Antitrypsin Deficiency ... National Human Genome Research Institute ... From the National Institutes of Health ... Alpha- ...
    https://www.genome.gov/.../Alpha-1-Antitrypsin-Deficiency - External Health Links
  4. About Antiphospholipid Syndrome (APS) From the National Institutes of Health (National Human Genome Research Institute)  
    Autoimmune Diseases/Specifics ... Autoimmune Diseases ... National Human Genome Research Institute ... From the National Institutes of Health ... Antiphospholipid Syndrome ...
    https://www.genome.gov/Genetic-Disorders/Antiphospholipid-Syndrome - External Health Links
  5. Familial hypobetalipoproteinemia 
    ... ANGPTL3 This condition is inherited in an autosomal codominant pattern. Codominance means that copies of the gene ...
    https://medlineplus.gov/.../familial-hypobetalipoproteinemia - Genetics
  6. Alpha-1 antitrypsin deficiency 
    ... SERPINA1 This condition is inherited in an autosomal codominant pattern. Codominance means that two different versions of ...
    https://medlineplus.gov/.../condition/alpha-1-antitrypsin-deficiency - Genetics
  7. Clopidogrel resistance 
    ... CYP2C19 Clopidogrel resistance is inherited in an autosomal codominant pattern. Codominance means that two different versions of ...
    https://medlineplus.gov/genetics/condition/clopidogrel-resistance - Genetics
  8. Thiopurine S-methyltransferase deficiency 
    ... is inherited in a pattern described as autosomal codominant. Codominance means that two different versions of the ...
    https://medlineplus.gov/...thiopurine-s-methyltransferase-deficiency - Genetics
  9. GeneReviews Glossary From the National Institutes of Health (National Center for Biotechnology Information)  
    Newborn Screening/Reference Desk ... Newborn Screening ... Genetic Testing/Reference Desk ... Genetic Testing ... National Center for Biotechnology Information ... From the National ...
    https://www.ncbi.nlm.nih.gov/books/NBK5191 - External Health Links