SM DIAGNOSTICS
NPI 1013930429
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.

2019-ncov coronavirus, sars-cov-2/2019-ncov (covid-19), any technique, multiple types or subtypes (includes all targets), non-cdc, making use of high throughput technologies as described by cms-2020-01-r

This service involves the testing for COVID-19 using advanced technologies that can process multiple samples at once. It identifies different types or subtypes of the virus, including SARS-CoV-2/2019-nCoV. This test is non-CDC but adheres to the guidelines outlined in CMS-2020-01-R.

This service was performed 27 times for 17 patients

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 389 times for 389 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 369 times for 369 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 18 times for 18 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 247 times for 247 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 15 times for 15 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 310 times for 310 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 307 times for 307 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 309 times for 309 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 284 times for 284 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 303 times for 303 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 279 times for 279 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 407 times for 406 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 394 times for 394 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 396 times for 396 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 303 times for 303 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 283 times for 283 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 404 times for 403 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 303 times for 303 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 30 times for 30 patients

Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, cdc or non-cdc, making use of high throughput technologies, completed within

This is a test to detect the COVID-19 virus. It uses a technique that amplifies the virus's genetic material (DNA or RNA) for detection. High throughput technologies are used for rapid and large-scale testing. The procedure is completed within a set time frame.

This service was performed 27 times for 17 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 12 times for 12 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 86 times for 79 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 151 times for 82 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 104 times for 82 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 51 times for 51 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 51 times for 51 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 51 times for 51 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 55 times for 55 patients

CLIA Information

The Clinical Laboratory Improvement Amendments (CLIA) of 1988 applies to facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease. The CLIA Program sets standards for clinical laboratory testing and issues certificates. The NPI / CLIA crosswalk information for this NPI number is:

CLIA Number

10D2262324

Facility Type

Independent

Certificate Effective Date

April 02, 2024

Certificate Expiration Date

April 01, 2026

Laboratory Director

DR. UZMA FAROOQ

Certificate Type

Certificate of Accreditation

Certificate Type Description

This is a CLIA certificate is issued to Sm Diagnostics on the basis of the laboratory's accreditation by an accreditation organization approved by CMS. This type of certificate is issued to a laboratories tha perform nonwaived (moderate and/or high complexity) testing.

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