ADVANCED DIAGNOSTICS LABORATORY LLC
NPI 1144716424
Clinical Medical Laboratory in Cherry Hill, NJ
NPI Status: Active since July 10, 2018
Contact Information
1030 KINGS HWY N STE 304
CHERRY HILL, NJ
ZIP 08034
Phone: (856) 320-2143
Fax: (856) 320-2147
- Organization
- Clinical Medical Laboratory
About ADVANCED DIAGNOSTICS LABORATORY LLC
This page provides the complete NPI Profile along with additional information for Advanced Diagnostics Laboratory Llc, a provider established in Cherry Hill, New Jersey operating as a Clinical Medical Laboratory. The healthcare provider is registered in the NPI registry with number 1144716424 assigned on July 2018. The practitioner's primary taxonomy code is 291U00000X with license number 0012217 (NJ). The provider is registered as an organization and their NPI record was last updated 2 years ago. The authorized official of this NPI record is Pamela R Baylin (Coo)
- NPI
- 1144716424
- Provider Name
- ADVANCED DIAGNOSTICS LABORATORY LLC
- Entity Type
- Organization
- Location Address
- 1030 KINGS HWY N STE 304 CHERRY HILL, NJ 08034
- Location Phone
- (856) 320-2143
- Location Fax
- (856) 320-2147
- Mailing Address
- 950 EAGLES LANDING PKWY # 133 STOCKBRIDGE, GA 30281
- Mailing Phone
- (856) 320-2143
- Mailing Fax
- (856) 320-2147
- Is Sole Proprietor?
- No
- Is Organization Subpart?
- No
- Enumeration Date
- 07-10-2018
- Last Update Date
- 01-11-2024
- Code Navigator
Establishments like Advanced Diagnostics Laboratory Llc 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
- License No.
- 0012217
- License State
- NJ
- 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.
Insurance Plans Accepted
According to publicly available information the provider might be accepting the following health plans from these health insurance companies:
Specific plan information not avaialable, please contact the provider to verify if your insurance plan is accepted.
Specific plan information not avaialable, please contact the provider to verify if your insurance plan is accepted.
*Please verify directly with this provider to make sure your insurance plan is currently accepted.
Additional Identifiers
The NPI Enumerator encourages providers to submit additional identifiers with their NPI application although the submission of this information is optional. The additional identifier(s) section includes other numbers or codes currently or formerly used as an identifier for the provider by other public healthcare entities. The identifiers may include UPIN, NSC, OSCAR, DEA, Medicaid State or PIN identification numbers.
| Identifier | Type / Code | Identifier State | Identifier Issuer |
|---|---|---|---|
| 2637037 | MEDICAID (05) | LA | |
| 003258190A | MEDICAID (05) | GA |
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 (coagulation factor ix) full sequence analysis
Gene analysis (coagulation factor v) leiden variant
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 c, polypeptide 9) 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 (glucose-6-phosphatase, catalytic subunit) common variants
Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis
Gene analysis (hemochromatosis) common variants
Gene analysis (janus kinase 2) targeted sequence analysis
Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10
Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis
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 (partner and localizer of brca2) full sequence analysis
Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis
Gene analysis (prothrombin, coagulation factor ii) a variant
Gene analysis (solute carrier organic anion transporter family, member 1b1) for common variant
Gene analysis of 16 genes to evaluate risk of opioid-use disorder
Molecular pathology procedure level 1
Molecular pathology procedure level 2
Molecular pathology procedure level 4
Molecular pathology procedure level 5
Molecular pathology procedure level 6 genetic analysis
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 739 times for 739 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 312 times for 312 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 76 times for 76 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 161 times for 161 patientsGene 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 236 times for 236 patientsGene 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 51 times for 51 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 85 times for 85 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 596 times for 596 patientsGene analysis for cytochrome P450 2C9 common variants is a test to identify specific genetic variations. These variations can affect how your body processes certain medications, helping to determine the most effective and safe drug dosage for you.
This service was performed 83 times for 83 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 516 times for 516 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 77 times for 77 patientsGene 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 77 times for 77 patientsGene 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 77 times for 77 patientsGene 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 741 times for 741 patientsGene 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 85 times for 85 patientsGene 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 85 times for 85 patientsGene 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 55 times for 55 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 313 times for 313 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 350 times for 350 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 406 times for 403 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 345 times for 345 patientsGene analysis for prothrombin (also known as coagulation factor II) is a test that examines your DNA to identify any variations in the prothrombin gene. These variations could potentially affect blood clotting, leading to an increased risk of certain health conditions.
This service was performed 51 times for 51 patientsGene analysis for the solute carrier organic anion transporter family, member 1b1 (SLCO1B1), common variant, is a test that examines your DNA to identify variations in the SLCO1B1 gene. This gene plays a crucial role in the body's ability to process certain medications.
This service was performed 95 times for 95 patientsThis service analyzes 16 specific genes to assess your potential risk for opioid-use disorder. It's a proactive measure to understand genetic predispositions, helping in personalizing medicine and prevention strategies.
This service was performed 228 times for 228 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 620 times for 620 patientsA 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 434 times for 217 patientsA 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 343 times for 172 patientsA 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 855 times for 172 patientsA 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 344 times for 172 patientsReviews for ADVANCED DIAGNOSTICS LABORATORY LLC
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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 1144716424, we treat the final digit (4) 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 56. The final step is to find the difference between that total and the next multiple of ten (60 - 56 = 4).
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 56 is 60. The difference is the calculated check digit.
Frequently Asked Questions
The NPI number assigned to this healthcare provider is 1144716424, enumerated as an "organization" on July 10, 2018.
The provider is located at 1030 KINGS HWY N STE 304 CHERRY HILL, NJ 08034 and the phone number is (856) 320-2143.
Clinical Medical Laboratory with taxonomy code 291U00000X.
The provider might be accepting Accepts: Medicare and Medicaid. Please consult your insurance carrier or call the provider to verify.
