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Lab Dept Chemistry Test Name TPMT GENOTYPE General Information Lab Order Codes TGEN Synonyms Prometheus TPMT Genetics Thiopurine S-methyltransferase Genetics CPT Codes 81401 Molecular pathology Level 2 Test Includes A qualitative evaluation to determine a patient s ability to produce thiopurine methyltransferase enzyme. Classifies patients into one of three genotypes normal wild type heterozygous or homozygous recessive. Logistics Test Indications Because each patient metabolizes thiopurines...
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The appearance refers to a class of drugs that suppress the normal activity of the body×39’s immune systecommonly prescribeded the appearing drugs include aids of via preen sold under the brand name in urine my captive hearing sold under the brand name pure Nassau and Thea guanine or 60g sold under the brand names tabloid or lands different the appearing drugs may be prescribed for different conditions a Sofia print or inuring is prescribed to prevent rejection after a kidney transplant and to reduce signs and symptoms of rheumatoid arthritis more captive purine or peer Ina Cell is prescribed as a maintenance therapy for acute lymphocytes leukemia and Thea guanine 60g or lambs is prescribed to induce remission inpatients with acute lymphocytes leukemia the appearing drugs may also be used to treat other autoimmune disorders including Crohn×39’s disease ulcerativecolitis and lupus when we take medication we usually take for granted that it will work in reality there is a lot that goes into how your body responds to a medication the appearing drugs are processed by the TPM enzyme the TPM gene tells the body how to make the TPM enzyme variants in the Imogene may impair the body's ability to process at the appearing drug causing into build up in the body if the appearing drugs build up in the body they can cause severe life-threatening side effects like bone marrow suppression bone marrow suppression is a severe decrease in cells responsible providing immunity carrying oxygen and those responsible for normal blood clotting each gene associated with drug metabolism including TPM is expected Mohave multiple sites of variation the appearing drug response is determined BYA combination of genetic variants or snips in the TPM gene each combination of genetic variants in or near a gene miscalled a haplotype there can be many combinations of variants for each gene to help identify the different combinations a numbering system is sometimes used in the example onecombinationvariance in the TPM gene may be called star one while another is called star three see the DNA sequence that makes an enzyme with normal or typical functions usually called star one since we have two copies of each gene one for mom anyone from dad each person will have combination of variants called haplotype from each parent when genetic testing is performed the results are noted as two numbers one representing each combination of variants in that gene were separated BYA slash for example someone who inherited the combination of variants from their father known as star one and the combination known as star 3c from their mother would be a star one slash star 3c for the TPM gene some people have combinations of variants that airfare and have not been studied or sometimes named the genetic test that is performed cannot determine a person'result with certainty haplotypes or combinations of genetic variants can reused to predict a person's TPM enzyme activity level for example someone with...

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TPMT (thiopurine methyltransferase) genetics product detail is a description and information about the specific genetic variations in the TPMT gene that may affect how individuals metabolize certain medications.
The requirement to file TPMT genetics product detail may vary depending on the specific regulations or guidelines set by regulatory authorities, healthcare institutions, or genetic testing laboratories. It is advisable to consult the relevant authorities or entities to determine who is required to file this information.
The process of filling out TPMT genetics product detail can vary depending on the specific requirements or forms provided by regulatory authorities, healthcare institutions, or genetic testing laboratories. Generally, it involves providing information about the specific genetic variations found in the TPMT gene, including details about the location, type of variation, and potential implications on medication metabolism. It is recommended to follow the instructions and guidelines provided by the relevant authorities or entities when filling out TPMT genetics product detail.
The purpose of TPMT genetics product detail is to provide healthcare professionals, regulatory authorities, and other relevant stakeholders with information about genetic variations in the TPMT gene that can affect how individuals metabolize certain medications. This information can help guide treatment decisions, personalize medication regimens, and minimize the risk of adverse drug reactions.
The specific information that must be reported on TPMT genetics product detail can vary depending on the requirements set by regulatory authorities, healthcare institutions, or genetic testing laboratories. Generally, it includes details about the specific genetic variations found in the TPMT gene, such as the location, type of variation (e.g., single nucleotide polymorphism), and the potential impact on medication metabolism or treatment decisions. The reporting requirements may also include patient information, testing methodology, and any additional guidance provided by the relevant authorities or entities.
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