UNITY HOLDING GROUPS LLC
NPI 1023720778
Clinical Medical Laboratory in Jessup, PA

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.

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 2,887 times for 2,887 patients

Gene analysis (additional sex combs like 1, transcriptional regulator) full sequence analysis

Gene analysis, specifically of the Additional Sex Combs Like 1, is a process where your DNA is examined to identify changes or alterations in a particular gene. This analysis helps to understand certain health conditions better and can guide treatment decisions.

This service was performed 23 times for 23 patients

Gene analysis (adenomatous polyposis coli), full gene sequence

Gene analysis of the adenomatous polyposis coli (APC) involves studying the entire sequence of the APC gene. This test helps identify mutations that could lead to conditions like familial adenomatous polyposis. The procedure is non-invasive and uses a blood sample.

This service was performed 881 times for 881 patients

Gene analysis (aspartoacylase)

Gene analysis for aspartoacylase is a test that studies your DNA to check for mutations in the ASPA gene. This gene is responsible for producing an enzyme called aspartoacylase, which plays a crucial role in brain development and function. Any changes could lead to health issues.

This service was performed 3,140 times for 3,140 patients

Gene analysis (ataxin 1) for abnormal alleles

Gene analysis of ataxin 1 involves studying your DNA to identify any abnormal versions of the ataxin 1 gene. This gene is associated with certain neurological disorders. The test helps in early detection and management of these conditions.

This service was performed 2,501 times for 2,501 patients

Gene analysis (ataxin 10) for abnormal alleles

Gene analysis for ataxin 10 involves examining your DNA to identify any abnormal versions of the ataxin 10 gene. These abnormalities could potentially cause certain health conditions. This test is non-invasive and helps in early detection and management of these conditions.

This service was performed 2,499 times for 2,499 patients

Gene analysis (ataxin 2) for abnormal alleles

Gene analysis for ataxin 2 checks for alterations in the ATXN2 gene. This gene is responsible for producing a protein essential for normal cell functions. If abnormal, it may lead to certain neurological disorders. The test involves analyzing your DNA, typically obtained via a blood sample.

This service was performed 2,491 times for 2,491 patients

Gene analysis (ataxin 3) for abnormal alleles

Gene analysis for ataxin 3 helps identify abnormal alleles, or variations, in the ataxin 3 gene. This gene plays a role in neurological function. If abnormal, it may indicate conditions like Machado-Joseph disease. The process involves analyzing a blood sample.

This service was performed 2,500 times for 2,500 patients

Gene analysis (ataxin 7) for abnormal alleles

Gene analysis for ataxin 7 involves studying your DNA to identify any unusual changes in the ataxin 7 gene. These changes, known as abnormal alleles, can cause health conditions like spinocerebellar ataxia. The test helps in early detection and management.

This service was performed 2,499 times for 2,499 patients

Gene analysis (ataxin 8 opposite strand [non-protein coding]) for abnormal alleles

Gene analysis for ataxin 8 opposite strand checks for unusual gene variants. This test helps identify genetic conditions that could affect your health. It involves analyzing your DNA, usually from a blood sample, to find these abnormal alleles.

This service was performed 2,515 times for 2,515 patients

Gene analysis (atropin 1) for abnormal alleles

Gene analysis for Atropin 1 involves studying your DNA to identify any unusual genetic variations. This test helps in understanding your genetic makeup better, which can aid in diagnosing or predicting certain health conditions.

This service was performed 2,323 times for 2,323 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 1,877 times for 1,877 patients

Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants

Gene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.

This service was performed 393 times for 393 patients

Gene analysis (breast cancer 2) of full sequence

Gene analysis (breast cancer 2) of full sequence is a test that studies your DNA to identify any changes or mutations in the genes associated with an increased risk of certain types of cancer.

This service was performed 51 times for 51 patients

Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence

Gene analysis of the calcium voltage-gated channel subunit alpha1 a involves examining your DNA to understand how your body regulates calcium. This helps identify potential health risks related to calcium imbalances. It's a non-invasive procedure involving a simple blood or saliva sample.

This service was performed 810 times for 810 patients

Gene analysis (ccaat/enhancer binding protein [c/ebp], alpha) full gene sequence

Gene analysis of the CCAAT/Enhancer Binding Protein (C/EBP), Alpha, involves studying the entire sequence of this particular gene. This can help identify variations or changes in the gene that might affect your health. This process is done in a lab using a sample of your cells.

This service was performed 11 times for 11 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 1,895 times for 1,895 patients

Gene analysis (coagulation factor v) leiden variant

Gene analysis for the coagulation factor V Leiden variant is a test to identify a specific genetic mutation. This mutation can increase the risk of developing abnormal blood clots in veins. The test involves analyzing a sample of your DNA, usually taken from a blood sample.

This service was performed 21 times for 21 patients

Gene analysis (cystatin b) of full sequence

Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.

This service was performed 3,126 times for 3,126 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 1,944 times for 1,944 patients

Gene analysis (dihydropyrimidine dehydrogenase) for common variant

Gene analysis for dihydropyrimidine dehydrogenase (DPD) common variant involves studying a specific gene in your body. This gene affects how your body processes certain medications. The test identifies any changes in this gene which may influence your response to these medications.

This service was performed 24 times for 24 patients

Gene analysis (enhancer of zeste 2 polycomb repressive complex 2 subunit) of full sequence

Gene analysis of the full sequence of the Enhancer of Zeste 2 Polycomb Repressive Complex 2 Subunit (EZH2) involves examining this specific gene in detail. This gene plays a crucial role in cell growth and division. The analysis helps identify any mutations that could potentially lead to health issues.

This service was performed 23 times for 23 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 3,395 times for 3,395 patients

Gene analysis (fragile x intellectual disability 2) for detection of abnormal alleles

Gene analysis for Fragile X Mental Retardation 2 involves studying your genetic material to identify any unusual changes in a specific gene. This can help determine if you have a particular genetic condition, or if you might pass it on to your children.

This service was performed 2,502 times for 2,502 patients

Gene analysis (fragile x syndrome, x-linked intellectual disability) for detection of abnormal alleles

Gene analysis for Fragile X Mental Retardation involves studying your DNA to identify any abnormal changes or 'alleles'. This helps in detecting the presence of Fragile X syndrome, a genetic condition that can cause learning and behavioral challenges.

This service was performed 2,497 times for 2,497 patients

Gene analysis (frataxin) of full sequence

Gene analysis of frataxin involves studying the entire sequence of the frataxin gene. This test helps identify any changes or mutations in the gene that may cause health issues, such as Friedreich's ataxia. It's a non-invasive procedure using a blood sample.

This service was performed 3,031 times for 3,031 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 2,668 times for 2,668 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 1,948 times for 1,948 patients

Gene analysis (glucosidase, beta, acid) common variants

Gene analysis of common variants in the beta-glucosidase acid enzyme helps understand certain health conditions. This enzyme plays a key role in the body's metabolism. By studying its variants, doctors can better diagnose and treat metabolic disorders.

This service was performed 3,131 times for 3,131 patients

Gene analysis (hemochromatosis) common variants

Gene analysis for hemochromatosis common variants is a test that checks for specific changes in your DNA. These changes could indicate a higher risk of developing hemochromatosis, a condition that causes your body to absorb too much iron from your diet.

This service was performed 3,063 times for 3,063 patients

Gene analysis (hemoglobin, subunit beta) full sequence analysis

Gene analysis of hemoglobin, subunit beta, is a detailed examination of a specific gene in your body. This test helps identify any changes or mutations that may lead to health conditions, such as blood disorders. It's a non-invasive procedure and a vital tool in personalized medicine.

This service was performed 819 times for 819 patients

Gene analysis (hexosaminidase a) common variants

Gene analysis of Hexosaminidase A common variants is a test that examines your DNA for changes in the Hex A gene. This gene is responsible for making an enzyme that breaks down certain substances in the body. Changes in this gene can lead to health issues.

This service was performed 3,125 times for 3,125 patients

Gene analysis (huntingtin) for abnormal alleles

Gene analysis for huntingtin examines your DNA to identify if you have abnormal versions of the huntingtin gene. These abnormal genes are associated with Huntington's disease, a nervous system disorder. This test helps in early detection and management.

This service was performed 2,327 times for 2,327 patients

Gene analysis (inhibitor of kappa light polypeptide gene enhancer in b-cells, kinase complex-associated protein) common variants

Gene analysis for common variants in the IKBKAP gene helps understand your body's response to certain medications. This non-invasive test studies your DNA to identify variations in this gene, which can influence drug effectiveness and safety.

This service was performed 3,139 times for 3,139 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 1,884 times for 1,884 patients

Gene analysis (methyl cpg binding protein 2) full sequence analysis

Gene analysis, specifically Methyl CpG Binding Protein 2 (MECP2) full sequence analysis, is a detailed examination of your DNA. This test focuses on the MECP2 gene, which plays a crucial role in nerve cell function and development. The results can help identify alterations or mutations that may cause certain health conditions.

This service was performed 816 times for 816 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) for detection of common variants

Gene analysis for the MPL proto-oncogene, thrombopoietin receptor, is a test that looks for common genetic variants. This helps in understanding certain health conditions related to blood cell production. It's a non-invasive procedure, involving a simple blood draw.

This service was performed 274 times for 274 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 1,885 times for 1,885 patients

Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis

Gene analysis, specifically for MUTL Homolog 1, linked to colon cancer, involves studying your DNA sequence. This helps identify any changes or mutations that might increase your risk of developing colon cancer. It's a preventive measure to manage potential health risks.

This service was performed 116 times for 116 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis

Gene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.

This service was performed 886 times for 886 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 2,828 times for 2,828 patients

Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant

Gene analysis for the p.Leu265Pro variant involves studying the MYD88 gene, which plays a crucial role in immune response. This test helps identify changes in this gene that could potentially cause health issues. It's a non-invasive procedure, done through a blood sample.

This service was performed 24 times for 24 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1) translocation analysis

Gene analysis, specifically neurotrophic receptor tyrosine kinase 1 (NTRK1) translocation analysis, is a test that examines your genes for specific changes. These changes could potentially lead to certain health conditions. This analysis helps in providing personalized treatment plans.

This service was performed 2,560 times for 2,560 patients

Gene analysis (neurotrophic receptor tyrosine kinase 2) translocation analysis

Gene analysis, specifically neurotrophic receptor tyrosine kinase 2 (NTRK2) translocation analysis, is a test that studies alterations in your genes. This analysis helps identify changes in the NTRK2 gene, which can sometimes be linked to certain health conditions. It's a vital part of personalized medicine.

This service was performed 2,560 times for 2,560 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 2,654 times for 2,654 patients

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

Gene analysis, specifically the partner and localizer of BRCA2 targeted sequence analysis, is a scientific procedure that studies specific parts of your DNA. It helps to identify if you have certain genetic changes that may increase your risk of developing specific health conditions.

This service was performed 2,553 times for 2,553 patients

Gene analysis (peripheral myelin protein 22), full sequence analysis

Gene analysis of peripheral myelin protein 22 involves studying the full sequence of this specific gene. This analysis helps identify any genetic variations that may lead to certain health conditions. It's a non-invasive test involving a simple blood draw or saliva sample.

This service was performed 3,121 times for 3,121 patients

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

Gene analysis, specifically phosphatase and tensin homolog (PTEN) full sequence analysis, is a test that looks at your DNA to identify any changes in the PTEN gene. This gene helps control cell growth and division. Changes may lead to certain health conditions.

This service was performed 184 times for 184 patients

Gene analysis (phospholipase c gamma 2) for common variants

Gene analysis for phospholipase C gamma 2 common variants is a test that checks for changes in the PLCG2 gene. These changes can sometimes lead to certain health conditions. The test uses a sample of your body's cells to analyze your DNA.

This service was performed 43 times for 43 patients

Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles

Gene analysis for Poly(A) Binding Protein Nuclear 1 (PABPN1) checks for abnormal alleles or variations in your DNA. This test can help identify genetic disorders caused by these variations. It's a non-invasive procedure, involving a simple blood or saliva sample.

This service was performed 2,495 times for 2,495 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 2,797 times for 2,797 patients

Gene analysis (protein phosphatase 2 regulatory subunit bbeta) for abnormal alleles

Gene analysis for the protein phosphatase 2 regulatory subunit Bbeta checks for unusual variations in your genes. This helps to identify potential health issues related to these genes. It's a simple, non-invasive test using a blood or saliva sample.

This service was performed 2,499 times for 2,499 patients

Gene analysis (runt related transcription factor 1) targeted sequence analysis

Gene analysis for RUNX1 involves studying a specific part of your DNA. This test helps identify changes or mutations in the RUNX1 gene, which can provide insights into certain health conditions. It's like reading a book to find any spelling mistakes that could change the story.

This service was performed 24 times for 24 patients

Gene analysis (survival of motor neuron 1, telomeric) for dosage/deletion

Gene analysis for survival of motor neuron 1 (SMN1) involves studying your DNA to identify changes or deletions in the SMN1 gene. This gene plays a key role in motor neuron health. Alterations can lead to conditions like spinal muscular atrophy. The process is safe and non-invasive.

This service was performed 726 times for 726 patients

Gene analysis (survival of motor neuron 1, telomeric) of full sequence

Gene analysis of the full sequence of Survival of Motor Neuron 1 (telomeric) is a test that examines your DNA to identify any changes in this specific gene. These changes could indicate conditions like Spinal Muscular Atrophy. It's a non-invasive procedure.

This service was performed 2,329 times for 2,329 patients

Gene analysis (tata box binding protein) for abnormal alleles

Gene analysis for the TATA box binding protein checks for abnormal alleles or variations in your DNA. This analysis helps identify potential genetic conditions. It's done by examining a sample of your cells, typically obtained through a blood draw or a cheek swab.

This service was performed 2,487 times for 2,487 patients

Gene analysis (telomerase reverse transcriptase) targeted sequence analysis

Gene analysis of telomerase reverse transcriptase (TERT) involves studying a specific segment of your DNA. It helps understand how your body's cells age and multiply, which can be crucial in diagnosing and managing certain health conditions.

This service was performed 22 times for 22 patients

Gene analysis (tumor protein 53) full sequence analysis

Gene analysis, specifically tumor protein 53 (TP53) full sequence analysis, is a test that examines the entire TP53 gene. This gene plays a key role in preventing cancer. If there are changes or mutations in this gene, it could lead to an increased risk of developing various types of cancer.

This service was performed 11 times for 11 patients

Gene analysis for cancer (neuroblastoma)

Gene analysis for neuroblastoma is a test that studies your genes to identify abnormalities linked to this type of cancer. It helps doctors tailor treatment plans, potentially improving outcomes and reducing side effects.

This service was performed 30 times for 30 patients

Gene analysis panel for evaluation of genes associated with epilepsy

A gene analysis panel for epilepsy evaluates specific genes linked to this condition. This test can help understand your epilepsy type and severity, potentially guiding treatment options. It involves a blood sample and lab analysis.

This service was performed 2,264 times for 2,264 patients

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