SM DIAGNOSTICS LLC
NPI 1689322232
Clinical Medical Laboratory in Miami, FL

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 (adenomatous polyposis coli), duplication or deletion variants

Gene analysis of the adenomatous polyposis coli is a test that detects changes in the APC gene. These changes may cause certain health conditions. Duplication or deletion variants refer to parts of the gene being repeated or missing. This information helps tailor treatment plans.

This service was performed 30 times for 30 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 31 times for 31 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 32 times for 32 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 98 times for 98 patients

Gene analysis (bruton's tyrosine kinase) for common variants

Gene analysis of Bruton's Tyrosine Kinase (BTK) for common variants is a test that examines your BTK gene. This gene plays a crucial role in the immune system. By studying it, we can identify any variations that might be linked to certain health conditions.

This service was performed 32 times for 32 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 31 times for 31 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 31 times for 31 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) duplication or deletion variants

Gene analysis for cystic fibrosis checks for duplication or deletion variants in the CFTR gene. These changes can affect the body's salt balance, leading to thick, sticky mucus in the lungs and other organs. This test helps in early detection and management of the disease.

This service was performed 32 times for 32 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 32 times for 32 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 31 times for 31 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 32 times for 32 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 32 times for 32 patients

Gene analysis (janus kinase 2) variant

Gene analysis (Janus Kinase 2 variant) is a test that examines your DNA to identify any changes in the JAK2 gene. This gene is crucial for blood cell production. If it's mutated, it can lead to various blood disorders. The test helps in diagnosing these conditions.

This service was performed 32 times for 32 patients

Gene analysis (kirsten rat sarcoma viral oncogene homolog), additional variants

Gene analysis of the Kirsten rat sarcoma viral oncogene homolog (KRAS) checks for extra variations in the KRAS gene. These variations may impact how your body responds to certain treatments. It's a non-invasive test, usually done on a blood or tissue sample.

This service was performed 32 times for 32 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 32 times for 32 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 32 times for 32 patients

Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) duplication or deletion variants

Gene analysis for MLH1 is a test that checks for changes in the MLH1 gene, which if altered, can increase the risk of colon cancer. Duplication or deletion variants refer to extra or missing copies of the gene. This can help in early detection and prevention.

This service was performed 214 times for 214 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 213 times for 213 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) duplication or deletion variants

Gene analysis for MUTS homolog 2 (colon cancer, nonpolyposis type 1) duplication or deletion variants is a test that looks for changes in a specific gene linked to a higher risk of colon cancer. It helps identify if you carry these gene changes, aiding in early detection and prevention.

This service was performed 212 times for 212 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 210 times for 210 patients

Gene analysis (muts homolog 6 [e coli]) duplication or deletion variants

Gene analysis (muts homolog 6 [e coli]) duplication or deletion variants is a genetic test. It identifies changes in your DNA that could indicate certain health conditions. This test looks specifically at the mutS homolog 6 gene for any duplications or deletions.

This service was performed 212 times for 212 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 203 times for 203 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 32 times for 32 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 264 times for 264 patients

Gene analysis (phosphatase and tensin homolog), duplication or deletion variant

Gene analysis for phosphatase and tensin homolog (PTEN) involves studying this specific gene for any duplications or deletions. These changes can impact health and may be associated with certain conditions. This test helps in understanding your genetic makeup better.

This service was performed 266 times for 266 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 266 times for 266 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 32 times for 32 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) duplication or deletion variants

Gene analysis for PMS2 duplication or deletion variants involves studying your DNA to detect changes in the PMS2 gene. This gene is important for DNA repair. Variations in this gene could potentially lead to certain health conditions. This test helps to identify these changes early.

This service was performed 212 times for 212 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 198 times for 198 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 32 times for 32 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 32 times for 32 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 271 times for 271 patients

Gene analysis (v-ki-ras2 kirsten rat sarcoma viral oncogene) variants in codons 12 and 13

Gene analysis for v-ki-ras2 kirsten rat sarcoma viral oncogene variants in codons 12 and 13 is a test to identify specific changes in your genes. These changes could potentially indicate a higher risk for certain types of cancer.

This service was performed 32 times for 32 patients

Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), d816 variants

Gene analysis of the V-KIT Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog, D816 variants, is a test performed on your DNA. This test helps identify changes or mutations in the KIT gene, which can be associated with certain health conditions.

This service was performed 240 times for 240 patients

Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), targeted sequence

Gene analysis of v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog (KIT) is a test that studies a specific gene associated with cell growth and development. It helps in identifying any alterations in this gene that may lead to health issues.

This service was performed 240 times for 240 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 32 times for 32 patients

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