NPI Details
ADVANCED DIAGNOSTICS LABORATORY LLC is a clinical medical laboratory in Cherry Hill, NJ. The provider is (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. ADVANCED DIAGNOSTICS LABORATORY LLC NPI is 1144716424. The provider is registered as an organization entity type.
The provider's business location address is:
1030 KINGS HWY N STE 304
CHERRY HILL, NJ
ZIP 08034-907
Phone: (856) 320-2143
Fax: (856) 320-2147
The provider's authorized official is Pamela R Baylin .
The authorized official title is Coo and has the following contact phone number (770) 371-7711.
The following top HCPCS codes were publicly reported for this provider under the Medicare program for the year 2016. The reported codes are based on the top codes for each available Medicare specialty, excluding evaluation and management codes.
- Molecular pathology procedure level 5 (HCPCS:81404)
- Gene analysis (hemochromatosis) common variants (HCPCS:81256)
- Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants (HCPCS:81291)
- Molecular pathology procedure level 1 (HCPCS:81400)
- Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants (HCPCS:81225)
- Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants (HCPCS:81226)
- Molecular pathology procedure level 2 (HCPCS:81401)
- Gene analysis (partner and localizer of brca2) full sequence analysis (HCPCS:81307)
- Gene analysis (muts homolog 6 [e coli]) full sequence analysis (HCPCS:81298)
- Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis (HCPCS:81317)
- Molecular pathology procedure level 6 genetic analysis (HCPCS:81405)
- Molecular pathology procedure level 4 (HCPCS:81403)
- Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis (HCPCS:81295)
- Gene analysis (adenomatous polyposis coli), full gene sequence (HCPCS:81201)
- Gene analysis (coagulation factor ix) full sequence analysis (HCPCS:81238)
- Gene analysis of 16 genes to evaluate risk of opioid-use disorder (HCPCS:0078U)
- Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants (HCPCS:81162)
- Gene analysis (solute carrier organic anion transporter family, member 1b1) for common variant (HCPCS:81328)
- Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 (HCPCS:81339)
- Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence (HCPCS:81223)
- Gene analysis (janus kinase 2) targeted sequence analysis (HCPCS:81279)
- Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 9) common variants (HCPCS:81227)
- Gene analysis (fanconi anemia, complementation group c) common variant (HCPCS:81242)
- Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis (HCPCS:81249)
- Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants (HCPCS:81250)
- Gene analysis (bloom syndrome, recq helicase-like) (HCPCS:81209)
- Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis (HCPCS:81292)
- Gene analysis (prothrombin, coagulation factor ii) a variant (HCPCS:81240)
- Gene analysis (coagulation factor v) leiden variant (HCPCS:81241)
The enumeration date for this NPI number is 7/10/2018 and was last updated on 1/11/2024.
Taxonomy Codes
The NPI record includes the healthcare provider taxonomy classification, state license number and state of licensure. The following information regarding the scope of practice of this provider is available:
| No. |
Taxonomy Code |
Taxonomy Clasification |
Taxonomy Specialization |
License Number |
License State |
Primary |
| 1 | 291U00000X | Clinical Medical Laboratory | | 0012217 | NEW JERSEY | Yes |
Other Identifiers
The following information regarding additional identifiers associated to this NPI record includes the other identifier number, identifier type, identifier state and issuer.
| No. |
Other Provider Identifier |
Other Provider Identifier Type |
Other Provider Identifier State |
Other Provider Identifier Issuer |
| 1 | 2637037 | MEDICAID | LOUISIANA | |
| 2 | 003258190A | MEDICAID | GEORGIA | |
