KINGDOM HEALTH LABORATORY LLC
NPI 1689264053
Clinical Medical Laboratory in Dallas, TX

Areas of Expertise

The following services and procedures, recently provided to Medicare patients, illustrate the range of care this provider offers. This list reflects the variety of services available to all patients visiting the practice and is based on 2022 Medicare dataset. In general, the more frequently a provider treats specific conditions or performs particular procedures, the more experienced they become in addressing similar patient needs. The provider has delivered many of the services listed below to Medicare patients. Please note that this list does not include services provided to patients who are not covered by Medicare.

Dna sequence analysis of mlh1, msh2, msh6, pms2, and epcam for lynch syndrome

DNA sequence analysis for Lynch syndrome checks the MLH1, MSH2, MSH6, PMS2, and EPCAM genes. These genes help fix DNA errors. If they're not working properly, it can lead to Lynch syndrome, increasing the risk of certain cancers.

This service was performed 16 times for 16 patients

Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants

Gene analysis for 5,10-methylenetetrahydrofolate reductase (MTHFR) common variants is a test that looks at your DNA to identify any changes in the MTHFR gene. These changes can affect how your body processes certain vitamins, which could impact your overall health.

This service was performed 152 times for 152 patients

Gene analysis (bloom syndrome, recq helicase-like)

Gene analysis for Bloom Syndrome involves studying the RECQ helicase-like gene. This gene is responsible for DNA repair. When it's not working properly, it can lead to Bloom Syndrome, a condition that increases the risk of developing various types of cancer.

This service was performed 34 times for 34 patients

Gene analysis (coagulation factor ix) full sequence analysis

Gene analysis for coagulation factor IX is a process that examines your genes, specifically the one responsible for factor IX - a protein that helps blood clot. It can detect any changes or mutations in this gene, which could affect your body's ability to control bleeding.

This service was performed 180 times for 180 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence

Gene analysis for cystic fibrosis involves examining the entire CFTR gene to identify any changes or mutations that could cause the disease. This can help in diagnosing and managing the condition effectively.

This service was performed 13 times for 13 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants

Gene analysis of cytochrome P450 2C19 common variants is a test that helps understand how your body processes certain medications. This can help your doctor tailor treatments specifically for you, improving their effectiveness and safety.

This service was performed 33 times for 33 patients

Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants

Gene analysis of cytochrome P450 2D6 (CYP2D6) common variants involves studying specific genes to understand your body's ability to process certain medications. This can help tailor treatments to your unique genetic makeup, optimizing medication effectiveness and safety.

This service was performed 53 times for 53 patients

Gene analysis (fanconi anemia, complementation group c) common variant

Gene analysis for Fanconi Anemia, Complementation Group C, is a test that looks at your DNA to see if you have changes in a specific gene linked to this type of anemia. This can help determine if you have the condition or if you might pass it on to your children.

This service was performed 13 times for 13 patients

Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants

Gene analysis of glucose-6-phosphatase, catalytic subunit, common variants involves studying specific genes related to glucose metabolism. This helps understand if you're at risk of certain metabolic disorders. It's a non-invasive procedure, involving a simple blood or saliva sample.

This service was performed 13 times for 13 patients

Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis

Gene analysis for glucose-6-phosphate dehydrogenase (G6PD) involves studying your DNA to check for changes in the G6PD gene. This gene controls an enzyme that helps red blood cells function properly. Anomalies can cause health issues like anemia.

This service was performed 19 times for 19 patients

Gene analysis (janus kinase 2) targeted sequence analysis

Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.

This service was performed 13 times for 13 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10

Gene analysis of the MPL proto-oncogene, thrombopoietin receptor, specifically sequence analysis of exon 10, is a procedure that studies a specific part of your DNA. It helps to identify any changes or mutations that may contribute to certain blood disorders.

This service was performed 13 times for 13 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis

Gene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.

This service was performed 13 times for 13 patients

Gene analysis (noonan syndrome) genomic sequence analysis

Gene analysis for Noonan Syndrome involves studying your DNA in detail. This helps identify any changes in specific genes associated with the syndrome. The process is non-invasive, involving a simple blood or saliva sample. The results can provide valuable information about your health.

This service was performed 685 times for 685 patients

Gene analysis (partner and localizer of brca2) full sequence analysis

Gene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.

This service was performed 52 times for 52 patients

Gene analysis (phosphatase and tensin homolog), full gene analysis

Gene analysis of phosphatase and tensin homolog (PTEN) is a test that studies your DNA to find changes in the PTEN gene. These changes could increase your risk for certain health conditions. It involves taking a blood or saliva sample for laboratory analysis.

This service was performed 16 times for 16 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis

Gene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.

This service was performed 41 times for 41 patients

Molecular pathology procedure level 2

A Molecular Pathology Procedure Level 2 is a laboratory test used to study genes at a molecular level. This helps identify genetic variations or mutations that may be associated with certain diseases or conditions. This information assists in diagnosing and managing your healthcare.

This service was performed 1,224 times for 739 patients

Molecular pathology procedure level 4

A Molecular Pathology Procedure Level 4 is a sophisticated lab test that analyzes your DNA. It helps identify specific genetic changes that may be causing or increasing the risk of certain diseases. This understanding can aid in diagnosis, treatment, and prevention strategies.

This service was performed 1,713 times for 710 patients

Molecular pathology procedure level 5

A Molecular Pathology Procedure Level 5 is a complex lab test that studies genes and proteins at a molecular level. It helps identify genetic changes or infections that may cause or influence disease. This information is crucial for diagnosis and treatment planning.

This service was performed 1,236 times for 711 patients

Molecular pathology procedure level 6 genetic analysis

A molecular pathology procedure level 6 genetic analysis is a complex lab test. It examines your DNA to identify specific genetic changes that can cause or increase the risk of disease. Understanding these changes can help in tailoring treatments.

This service was performed 1,426 times for 711 patients

Test for detecting genes associated with colon cancer, genomic sequence analysis panel, at least 10 genes

This is a genetic test that checks for specific genes linked to colon cancer. The test analyzes a minimum of 10 genes to identify any changes or mutations that may increase the risk of developing this type of cancer.

This service was performed 33 times for 33 patients

Test for detecting genes associated with heart disease, duplication/deletion analysis panel

This test identifies genetic markers linked to heart disease. The duplication/deletion analysis panel scans your DNA for changes that may increase your risk. Understanding your genetic profile can help manage potential heart health risks.

This service was performed 661 times for 661 patients

Test for detecting genes associated with heart disease, duplication/deletion analysis panel, at least 2 genes

This test checks your DNA for changes in at least 2 genes linked to heart disease. It helps identify if you have a higher risk of developing heart conditions. The duplication/deletion analysis looks for extra or missing pieces in these genes.

This service was performed 668 times for 668 patients

Test for detecting genes associated with heart disease, genomic sequence analysis panel, at least 10 genes

This test identifies genetic variations linked to heart disease. It involves analyzing a panel of 10 genes. Genetic material is extracted from a blood sample and examined for changes that could indicate a higher risk of developing heart conditions.

This service was performed 668 times for 668 patients

Test for detecting genes associated with heart disease, genomic sequence analysis panel, at least 9 genes

This test analyzes at least 9 specific genes associated with heart disease. It uses a method called genomic sequencing to identify potential genetic risks. Understanding these risks can help in managing heart health more effectively.

This service was performed 685 times for 685 patients

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