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Results 11 - 20 of 1,563 for genetic ACID
  1. Metabolic Disorders (National Library of Medicine)  
    ... of disorders. Some affect the breakdown of amino acids, carbohydrates, or ... become diseased or do not function normally. Diabetes is an example.
    https://medlineplus.gov/metabolicdisorders.html - Health Topics
  2. Congenital bile acid synthesis defect type 1 
    Congenital bile acid synthesis defect type 1 is a disorder characterized by cholestasis, a condition that impairs the production and release of a digestive fluid ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-1 - Genetics
  3. Congenital bile acid synthesis defect type 2 
    ... delta(4)-3-oxosteroid 5-beta-reductase deficiency Genetic Testing Registry: Congenital bile acid synthesis defect 2 Congenital bile acid synthesis defect ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  4. RERE gene 
    ... type of mutation in the RERE gene. Additional genetic factors that have not been identified, ... ARG arginine-glutamic acid dipeptide (RE) repeats arginine-glutamic acid repeats-encoding ...
    https://medlineplus.gov/genetics/gene/rere - Genetics
  5. Degenerative Nerve Diseases (National Library of Medicine)  
    Degenerative nerve diseases affect many of your body's activities, such as balance, movement, talking, breathing, and heart function. Many of these diseases are genetic. ...
    https://medlineplus.gov/degenerativenervediseases.html - Health Topics
  6. CNBP gene 
    The CNBP gene provides instructions for making a protein called CCHC-type zinc finger nucleic acid binding protein. This protein has seven regions, called ...
    https://medlineplus.gov/genetics/gene/cnbp - Genetics
  7. FA2H gene 
    ... article on PubMed Central Gregory A, Hayflick SJ. Genetics of ... SJ. Fatty Acid Hydroxylase-Associated Neurodegeneration. 2011 Jun 28 [updated 2018 ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
  8. ALAD gene 
    ... Sexton MJ, Fowler BA. Lead and delta-aminolevulinic acid dehydratase polymorphism: where does it lead? A meta-analysis. Environ Health Perspect. 2007 Jan;115(1):35-41. doi: 10.1289/ehp.9448. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/alad - Genetics
  9. ACP5 gene 
    ... J, Unger S, Zabel B, Superti-Furga A. Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and ...
    https://medlineplus.gov/genetics/gene/acp5 - Genetics
  10. Maple syrup urine disease 
    ... the condition. BCKD deficiency Branched-chain alpha-keto acid dehydrogenase deficiency Branched-chain ketoaciduria Ketoacidemia MSUD Genetic Testing Registry: Classical maple syrup urine disease Genetic ...
    https://medlineplus.gov/genetics/condition/maple-syrup-urine-disease - Genetics
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