EXPRESS GENE MOLECULAR DIAGNOSTICS LABORATORY
NPI 1184255606
Clinical Medical Laboratory in Palmetto Bay, FL

NPI Status: Active since February 03, 2020

Contact Information

9000 SW 152ND ST STE 209
PALMETTO BAY, FL
ZIP 33157
Phone: (786) 250-3419
Fax: (786) 250-3074

Get Directions Write a Review

  • Organization
  • Clinical Medical Laboratory
  • CLIA Number: 10D2178891
  • CLIA Cert. Type: Independent
  • CLIA Exp. Date: 05-07-2028

About EXPRESS GENE MOLECULAR DIAGNOSTICS LABORATORY

This page provides the complete NPI Profile along with additional information for Express Gene Molecular Diagnostics Laboratory, a provider established in Palmetto Bay, Florida operating as a Clinical Medical Laboratory. The healthcare provider is registered in the NPI registry with number 1184255606 assigned on February 2020. The practitioner's primary taxonomy code is 291U00000X. The provider is registered as an organization and their NPI record was last updated 6 years ago. The provider's is doing business as Express Gene Molecular Diagnostics Laboratory. The authorized official of this NPI record is Dr. Mohammad Ali Faghihi M.d., Ph.d. (Laboratory Director)

NPI
1184255606
Provider Legal Name
EXPRESS GENE LLC
Other Organization Name
EXPRESS GENE MOLECULAR DIAGNOSTICS LABORATORY
Other Name Type
Doing Business As (3)
Entity Type
Organization
Location Address
9000 SW 152ND ST STE 209 PALMETTO BAY, FL 33157
Location Phone
(786) 250-3419
Location Fax
(786) 250-3074
Mailing Address
9000 SW 152ND STREET SUITE 209 PALMETTO BAY, FL 33157
Mailing Phone
(786) 250-3419
Mailing Fax
(786) 250-3074
Is Sole Proprietor?
No
Is Organization Subpart?
No
Enumeration Date
02-03-2020
Last Update Date
02-04-2020
Code Navigator

Establishments like Express Gene Molecular Diagnostics Laboratory are healthcare facilities that may perform a wide range of laboratory procedures, assisted by doctors and medical technologists. Laboratories can be categorized according to their function as common diagnostic labs or specialty labs that conduct specialized or confirmatory tests. Different clinical laboratories could specialize in clinical chemistry, clinical microbiology, hematology, serology, clinical microscopy, cytopathology, molecular biology, or public health. Please inquire directly with this provider to confirm their test menu.

Clinical labs in the U.S. that perform human testing are regulated by the Centers for Medicare & Medicaid Services (CMS) through the Clinical Laboratory Improvement Amendments (CLIA) program. The purpose of the CLIA program is to guarantee the quality of laboratory testing. This provider has a CLIA number assigned, and undergoes regular inspections to ensure compliance and quality.

Location Map

Specialty - Primary Taxonomy

The NPI enumerator requires providers to submit at least one taxonomy code. A taxonomy code is a unique 10-character code that describes the healthcare provider type, classification, and the area of specialization. There could be only one primary taxonomy code per NPI record. For individual NPIs the license data is associated to the taxonomy code.

Classification

Clinical Medical Laboratory

Taxonomy Code
291U00000X
Type
Laboratories
Taxonomy Description
(1) A clinical laboratory is a facility for the biological, microbiological, serological, chemical, immunohematological, hematological, biophysical, cytological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, human beings. These examinations also include procedures to determine, measure, or otherwise describe the presence or absence of various substances or organisms in the body. Facilities only collecting or preparing specimens (or both) or only serving as a mailing service and not performing testing are not considered clinical laboratories. (2) Any facility that examines materials from the human body for purposes of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of, the health of human beings. Typical divisions of a clinical laboratory include hematology, cytology, bacteriology, histology, biochemistry, medical toxicology, and serology.

Authorized Official

The authorized official is the designated individual with the legal authority to make changes to the provider’s official NPI record. For organizations, the authorized official must be a general partner, chairman of the board, CEO, CFO or a direct owner holding at least a 5 percent stake in the medical organization.

Authorized Official Name

DR. MOHAMMAD ALI FAGHIHI M.D., PH.D.

Authorized Official Title
LABORATORY DIRECTOR
Authorized Official Phone
(786) 250-3419

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 (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 58 times for 58 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 59 times for 59 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 57 times for 57 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 59 times for 59 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 61 times for 61 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 58 times for 58 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 58 times for 58 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 60 times for 60 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 58 times for 58 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 59 times for 59 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 59 times for 59 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 59 times for 59 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 59 times for 59 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1, 2, and 3) translocation analysis

Gene analysis for neurotrophic receptor tyrosine kinase (NTRK) 1, 2, and 3 translocation is a test that checks for changes in your genes. These changes can impact how cells grow and divide, which can affect your health. It's a way to catch problems early.

This service was performed 11 times for 11 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 58 times for 58 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 58 times for 58 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 61 times for 61 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 59 times for 59 patients

Gene analysis (septin9) for promoter methylation

Gene analysis (Septin9) for promoter methylation is a non-invasive procedure that examines your DNA to identify certain changes or abnormalities. This specific test focuses on the Septin9 gene, which, when altered, may indicate a higher risk for certain health conditions.

This service was performed 59 times for 59 patients

Gene analysis (serpin peptidase inhibitor, clade a, alpha-1 antiproteinase, antitrypsin, member 1) common variants

Gene analysis for SERPINA1 common variants is a test that checks for changes in the SERPINA1 gene. This gene helps protect your lungs and liver from damage. Certain changes can lead to conditions like lung disease or liver problems. This test helps identify those changes.

This service was performed 11 times for 11 patients

Gene analysis (sphingomyelin phosphodiesterase 1, acid lysosomal) common variants

Gene analysis of sphingomyelin phosphodiesterase 1, acid lysosomal, involves studying specific variants in your genes. This helps understand your body's enzyme production, which can influence health conditions. It's a non-invasive procedure using a simple blood or saliva sample.

This service was performed 11 times for 11 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 62 times for 62 patients

Gene analysis (transforming growth factor beta-induced) for common variants

Gene analysis for common variants in the transforming growth factor beta-induced (TGFBI) gene helps understand your genetic makeup better. This procedure checks for variations in the TGFBI gene, which can influence your health. It's a safe, non-invasive test that uses a simple blood or saliva sample.

This service was performed 61 times for 61 patients

Gene analysis (v-raf murine sarcoma viral oncogene homolog b1)

Gene analysis of v-raf murine sarcoma viral oncogene homolog b1 (BRAF) is a test that examines your DNA to identify changes or mutations in the BRAF gene. This information can help in diagnosing and treating certain diseases, including some types of cancer.

This service was performed 59 times for 59 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 61 times for 61 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 11 times for 11 patients

Provision of covid-19 test, nonprescription self-administered and self-collected use, fda approved, authorized or cleared, one test count

This service provides a FDA-approved COVID-19 test kit for personal use. The test is self-administered and self-collected, meaning you conduct the test yourself. The kit contains all necessary items for one test. Follow the instructions carefully to ensure accurate results.

This service was performed 44,952 times for 4,654 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
10D2178891
Facility Type
Independent
Certificate Effective Date
May 08, 2026
Certificate Expiration Date
May 07, 2028
Laboratory Director
DR. MOHAMMAD FAGHIHI
Certificate Type
Certificate of Accreditation
Certificate Type Description
This is a CLIA certificate is issued to Express Gene Molecular Diagnostics Laboratory 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.

Reviews for EXPRESS GENE MOLECULAR DIAGNOSTICS LABORATORY

There are currently no reviews for this provider. Be the first person to share your experience with this provider by filling out our review form. Your insights are appreciated and will help others make informed decisions.

NPI NPI Number Validation

How NPI Validation Works

The NPI validation process uses the ISO-standard Luhn algorithm, a mathematical "handshake", to ensure that a provider's 10-digit ID is authentic and free of common typing errors.

To verify the NPI 1184255606, we treat the final digit (6) as the Check Digit—the target answer we need to reach. The process begins by taking the first nine digits and adding a constant value of 24, which accounts for the "80840" prefix required for all U.S. health identifiers. We then double every other digit starting from the right and sum the individual digits of those results together. For this specific NPI, that total comes to 54. The final step is to find the difference between that total and the next multiple of ten (60 - 54 = 6).

Digit-by-digit view

Use the first nine digits for the calculation. Starting from the right, double every other digit. The last digit is the check digit and is not part of the calculation.

Pos 1
1
Doubled → 2
Pos 2
1
Unchanged
Pos 3
8
Doubled → 16 → 1 + 6
Pos 4
4
Unchanged
Pos 5
2
Doubled → 4
Pos 6
5
Unchanged
Pos 7
5
Doubled → 10 → 1 + 0
Pos 8
6
Unchanged
Pos 9
0
Doubled → 0
Check
6
Target digit
Regular digit Doubled digit Check digit

Step 1: Double every other digit from the right

Starting with the rightmost digit of the first nine digits, double every other value. If doubling creates a two-digit number, add those digits together.

1 → 2 8 → 16 → 7 2 → 4 5 → 10 → 1 0 → 0

Step 2: Add all digits plus the NPI constant

Add the transformed values, the unchanged digits, and the constant 24.

2 + 1 + 1 + 6 + 4 + 4 + 5 + 1 + 0 + 6 + 0 + 24 = 54

Step 3: Find the amount needed to reach the next multiple of 10

The next multiple of ten after 54 is 60. The difference is the calculated check digit.

60 - 54 = 6
This NPI is valid
The calculated check digit is 6, which matches the last digit of 1184255606.

Other Providers at the Same Location


The following 1 provider is registered at the same or a nearby location.

Pathology (Molecular Genetic Pathology)
9000 SW 152ND ST STE 209
PALMETTO BAY, FL 33157

Frequently Asked Questions

The NPI number assigned to this healthcare provider is 1184255606, enumerated as an "organization" on February 03, 2020.

The provider is located at 9000 SW 152ND ST STE 209 PALMETTO BAY, FL 33157 and the phone number is (786) 250-3419.

Clinical Medical Laboratory with taxonomy code 291U00000X.