ADVAGENIX
NPI 1538618632
Clinical Medical Laboratory in Rockville, MD
NPI Status: Active since September 30, 2016
Contact Information
9430 KEY WEST AVE
SUITE 130
ROCKVILLE, MD
ZIP 20850
Phone: (301) 358-3564
Fax: (240) 747-7300
- Organization
- Clinical Medical Laboratory
About ADVAGENIX
This page provides the complete NPI Profile along with additional information for Advagenix, a provider established in Rockville, Maryland operating as a Clinical Medical Laboratory. The healthcare provider is registered in the NPI registry with number 1538618632 assigned on September 2016. The practitioner's primary taxonomy code is 291U00000X. The provider is registered as an organization and their NPI record was last updated 7 years ago. The authorized official of this NPI record is Dr. William G Kearns (President)
- NPI
- 1538618632
- Provider Name
- ADVAGENIX
- Entity Type
- Organization
- Location Address
- 9430 KEY WEST AVE SUITE 130 ROCKVILLE, MD 20850
- Location Phone
- (301) 358-3564
- Location Fax
- (240) 747-7300
- Mailing Address
- 9430 KEY WEST AVE SUITE 130 ROCKVILLE, MD 20850
- Mailing Phone
- (301) 358-3564
- Mailing Fax
- (240) 747-7300
- Is Sole Proprietor?
- No
- Is Organization Subpart?
- No
- Enumeration Date
- 09-30-2016
- Last Update Date
- 04-02-2019
- Code Navigator
Establishments like Advagenix 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.
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.
Secondary Taxonomies
The provider has reported to the NPI enumerator additional taxonomy codes. Multiple taxonomy codes may represent subspecialties or other areas of specialization the provider maybe licensed to practice.
| No. | Taxonomy Code | Type | Classification / Specialization |
License No. (State) |
|---|---|---|---|---|
| 1 | 261QG0250X | Ambulatory Health Care Facilities | Clinic/Center |
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 (adenomatous polyposis coli), full gene sequence
Gene analysis (bloom syndrome, recq helicase-like)
Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants
Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence
Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants
Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants
Gene analysis (fanconi anemia, complementation group c) common variant
Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis
Gene analysis (muts homolog 6 [e coli]) full sequence analysis
Gene analysis (neurotrophic receptor tyrosine kinase 1) translocation analysis
Gene analysis (partner and localizer of brca2) full sequence analysis
Gene analysis (partner and localizer of brca2) targeted sequence analysis
Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis
Molecular pathology procedure level 1
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 33 times for 33 patientsGene 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 43 times for 43 patientsGene 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 19 times for 19 patientsGene 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 14 times for 14 patientsGene 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 34 times for 34 patientsGene 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 14 times for 14 patientsGene 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 19 times for 19 patientsGene 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 27 times for 27 patientsGene 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 19 times for 19 patientsGene 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 19 times for 19 patientsGene 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 19 times for 19 patientsGene 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 19 times for 19 patientsGene 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 19 times for 19 patientsGene 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 42 times for 42 patientsA Molecular Pathology Procedure Level 1 is a lab test that studies the genes in your cells. It helps identify alterations in your DNA that may cause or contribute to certain diseases. The procedure is non-invasive and helps in early disease detection.
This service was performed 68 times for 34 patientsReviews for ADVAGENIX
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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 1538618632, we treat the final digit (2) 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 68. The final step is to find the difference between that total and the next multiple of ten (70 - 68 = 2).
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.
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.
Step 2: Add all digits plus the NPI constant
Add the transformed values, the unchanged digits, and the constant 24.
Step 3: Find the amount needed to reach the next multiple of 10
The next multiple of ten after 68 is 70. The difference is the calculated check digit.
Other Providers at the Same Location
The following 1 provider is registered at the same or a nearby location.
Frequently Asked Questions
The NPI number assigned to this healthcare provider is 1538618632, enumerated as an "organization" on September 30, 2016.
The provider is located at 9430 KEY WEST AVE SUITE 130 ROCKVILLE, MD 20850 and the phone number is (301) 358-3564.
Clinical Medical Laboratory with taxonomy code 291U00000X.
