PRISM MOLECULAR LLC
NPI 1558067199
Clinical Medical Laboratory in Blakely, PA

Q: What is Prism Molecular LLC's NPI number?

The NPI number for Prism Molecular LLC is 1558067199. It was assigned to this organization in the NPPES registry on February 6, 2023.

Q: What is Prism Molecular LLC's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

Active since February 06, 2023

1801 MAIN ST STE 104, BLAKELY, PA 18447(570) 382-8125 Get Directions Write a Review

NPPES record last updated: April 1, 2024. Verified against the NPPES registry weekly; last sync: August 02, 2026.

Record update history: Apr 1, 2024, Feb 6, 2023 (2 updates tracked since 2023).

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About Prism Molecular Llc NPPES

Official registry information on file with the National Plan and Provider Enumeration System.

PRISM MOLECULAR LLC (NPI 1558067199) is a healthcare organization registered as a clinical medical laboratory in Blakely, Pennsylvania and active in the NPI registry since February 2023. The organization lists Howard M Wegman, President, as its authorized official.

NPPES Registry Identity

NPI1558067199

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NamePRISM MOLECULAR LLC

Location Address1801 MAIN ST STE 104Blakely, PA 18447-1365

Mailing Address140 Enchanted Pkwy Ste 202Manchester, MO 63021-5491 · (314) 952-3261

Phone(570) 382-8125

Organization SubpartNo

Authorized OfficialHoward M WegmanPresident · (314) 952-2370

Enumeration DateFebruary 6, 2023

Last NPPES UpdateApril 1, 20242 updates tracked since enumeration

NPPES CertifiedMarch 27, 2024

✔ NPI 1558067199 is a valid, active identifier and passes the ISO check-digit test.

Specialties & Licenses

★ Primary SpecialtyClinical Medical LaboratoryLaboratories

Taxonomy Code291U00000X

Definition

(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.

1801 MAIN ST STE 104, Blakely, PA 18447

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Areas of Expertise CMS Part B claims 49

Services this provider delivered to Medicare fee-for-service patients, from the CMS Medicare utilization data. Higher counts generally reflect more experience with a service; care delivered outside Medicare is not included.

Detection test by nucleic acid for organism, amplified probe technique 87798

A nucleic acid detection test is a procedure to identify specific organisms in your body. This test uses an amplified probe technique, which magnifies the genetic material of the organism, making it easier to detect. It's a precise way to diagnose infections.

44,273 services1,024 patients

Detection test for candida species (yeast), amplified probe technique 87481

This test helps identify Candida, a type of fungus often present in the human body. An amplified probe technique is used, which enhances detection of the fungus in a sample. This method increases the accuracy of the test, helping to determine the best treatment.

4,672 services653 patients

Detection test by nucleic acid for staphylococcus aureus (bacteria), amplified probe technique 87640

A detection test for Staphylococcus aureus uses a method called the amplified probe technique. This method identifies the bacteria's unique genetic material, or nucleic acid, helping to confirm its presence. It's a highly accurate way to detect this type of bacteria.

4,201 services1,025 patients

Detection test by nucleic acid for multiple types of respiratory virus, multiple types or subtypes, 3-5 targets 87631

This test identifies different respiratory viruses by examining their nucleic acid, the building blocks of their genetic material. It can detect multiple types or subtypes, specifically 3-5 targets. This helps in diagnosing your respiratory illness accurately.

2,872 services820 patients

Detection test by nucleic acid for vancomycin resistance strep (vre), amplified probe technique 87500

The detection test by nucleic acid for vancomycin-resistant strep (VRE) is a laboratory procedure. It uses an amplified probe technique to identify specific genetic material in bacteria. This helps determine if the bacteria are resistant to the antibiotic vancomycin.

1,956 services820 patients

Detection test by nucleic acid for staphylococcus aureus, methicillin resistant (mrsa bacteria), amplified probe technique 87641

A detection test by nucleic acid for MRSA bacteria uses an amplified probe technique. It's a lab procedure that identifies the presence of MRSA, a type of bacteria resistant to many antibiotics. This test helps in deciding the best treatment.

1,955 services820 patients

Detection test by nucleic acid for strep (streptococcus, group a), amplified probe technique 87651

This test detects Group A Streptococcus bacteria in your body. It uses an amplified probe technique, which amplifies the bacteria's nucleic acid, making it easier to identify. This test helps diagnose conditions like strep throat or scarlet fever.

1,160 services653 patients

Detection test by nucleic acid for strep (streptococcus, group b), amplified probe technique 87653

A detection test by nucleic acid for Group B Strep uses an amplified probe technique. This test identifies the presence of Group B Strep bacteria in the body. It involves collecting a sample, usually a swab, which is then examined in a lab for the bacteria's genetic material.

1,160 services653 patients

Detection test by nucleic acid for human papillomavirus (hpv), high-risk types 87624

This test detects high-risk types of HPV, a common virus. It's done by analyzing a small sample of cells for the presence of HPV DNA. The aim is to identify any high-risk types early, as they may increase the risk of certain health issues.

1,078 services646 patients

Genomic sequence analysis panel for severe inherited conditions with sequencing of 15 or more genes 81443

This procedure involves analyzing your genetic material to identify specific mutations that could cause severe inherited conditions. It examines 15 or more genes. The information can help in diagnosis, treatment planning, and understanding your risk for certain diseases.

240 services231 patients

Gene analysis panel for evaluation of genes associated with epilepsy 81419

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.

187 services187 patients

Gene analysis (ataxin 1) for abnormal alleles 81178

Gene analysis of ataxin 1 involves studying your DNA to identify any abnormal versions of the ataxin 1 gene. This gene is associated with certain neurological disorders. The test helps in early detection and management of these conditions.

186 services186 patients

Gene analysis (ataxin 2) for abnormal alleles 81179

Gene analysis for ataxin 2 checks for alterations in the ATXN2 gene. This gene is responsible for producing a protein essential for normal cell functions. If abnormal, it may lead to certain neurological disorders. The test involves analyzing your DNA, typically obtained via a blood sample.

186 services186 patients

Gene analysis (ataxin 3) for abnormal alleles 81180

Gene analysis for ataxin 3 helps identify abnormal alleles, or variations, in the ataxin 3 gene. This gene plays a role in neurological function. If abnormal, it may indicate conditions like Machado-Joseph disease. The process involves analyzing a blood sample.

186 services186 patients

Gene analysis (ataxin 8 opposite strand [non-protein coding]) for abnormal alleles 81182

Gene analysis for ataxin 8 opposite strand checks for unusual gene variants. This test helps identify genetic conditions that could affect your health. It involves analyzing your DNA, usually from a blood sample, to find these abnormal alleles.

186 services186 patients

Gene analysis (ataxin 10) for abnormal alleles 81183

Gene analysis for ataxin 10 involves examining your DNA to identify any abnormal versions of the ataxin 10 gene. These abnormalities could potentially cause certain health conditions. This test is non-invasive and helps in early detection and management of these conditions.

186 services186 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1) translocation analysis 81191

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.

186 services186 patients

Gene analysis (neurotrophic receptor tyrosine kinase 2) translocation analysis 81192

Gene analysis, specifically neurotrophic receptor tyrosine kinase 2 (NTRK2) translocation analysis, is a test that studies alterations in your genes. This analysis helps identify changes in the NTRK2 gene, which can sometimes be linked to certain health conditions. It's a vital part of personalized medicine.

186 services186 patients

Gene analysis (fragile x syndrome, x-linked intellectual disability) for detection of abnormal alleles 81243

Gene analysis for Fragile X Mental Retardation involves studying your DNA to identify any abnormal changes or 'alleles'. This helps in detecting the presence of Fragile X syndrome, a genetic condition that can cause learning and behavioral challenges.

186 services186 patients

Gene analysis (glucosidase, beta, acid) common variants 81251

Gene analysis of common variants in the beta-glucosidase acid enzyme helps understand certain health conditions. This enzyme plays a key role in the body's metabolism. By studying its variants, doctors can better diagnose and treat metabolic disorders.

186 services186 patients

Gene analysis (hexosaminidase a) common variants 81255

Gene analysis of Hexosaminidase A common variants is a test that examines your DNA for changes in the Hex A gene. This gene is responsible for making an enzyme that breaks down certain substances in the body. Changes in this gene can lead to health issues.

186 services186 patients

Gene analysis (inhibitor of kappa light polypeptide gene enhancer in b-cells, kinase complex-associated protein) common variants 81260

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.

186 services186 patients

Gene analysis (huntingtin) for abnormal alleles 81271

Gene analysis for huntingtin examines your DNA to identify if you have abnormal versions of the huntingtin gene. These abnormal genes are associated with Huntington's disease, a nervous system disorder. This test helps in early detection and management.

186 services186 patients

Gene analysis (frataxin) of full sequence 81286

Gene analysis of frataxin involves studying the entire sequence of the frataxin gene. This test helps identify any changes or mutations in the gene that may cause health issues, such as Friedreich's ataxia. It's a non-invasive procedure using a blood sample.

186 services186 patients

Gene analysis (survival of motor neuron 1, telomeric) of full sequence 81336

Gene analysis of the full sequence of Survival of Motor Neuron 1 (telomeric) is a test that examines your DNA to identify any changes in this specific gene. These changes could indicate conditions like Spinal Muscular Atrophy. It's a non-invasive procedure.

186 services186 patients

Gene analysis (tata box binding protein) for abnormal alleles 81344

Gene analysis for the TATA box binding protein checks for abnormal alleles or variations in your DNA. This analysis helps identify potential genetic conditions. It's done by examining a sample of your cells, typically obtained through a blood draw or a cheek swab.

186 services186 patients

Gene analysis (fragile x intellectual disability 2) for detection of abnormal alleles 81171

Gene analysis for Fragile X Mental Retardation 2 involves studying your genetic material to identify any unusual changes in a specific gene. This can help determine if you have a particular genetic condition, or if you might pass it on to your children.

185 services185 patients

Gene analysis (atropin 1) for abnormal alleles 81177

Gene analysis for Atropin 1 involves studying your DNA to identify any unusual genetic variations. This test helps in understanding your genetic makeup better, which can aid in diagnosing or predicting certain health conditions.

185 services185 patients

Gene analysis (aspartoacylase) 81200

Gene analysis for aspartoacylase is a test that studies your DNA to check for mutations in the ASPA gene. This gene is responsible for producing an enzyme called aspartoacylase, which plays a crucial role in brain development and function. Any changes could lead to health issues.

185 services185 patients

Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles 81312

Gene analysis for Poly(A) Binding Protein Nuclear 1 (PABPN1) checks for abnormal alleles or variations in your DNA. This test can help identify genetic disorders caused by these variations. It's a non-invasive procedure, involving a simple blood or saliva sample.

185 services185 patients

Gene analysis (peripheral myelin protein 22), full sequence analysis 81325

Gene analysis of peripheral myelin protein 22 involves studying the full sequence of this specific gene. This analysis helps identify any genetic variations that may lead to certain health conditions. It's a non-invasive test involving a simple blood draw or saliva sample.

185 services185 patients

Gene analysis (protein phosphatase 2 regulatory subunit bbeta) for abnormal alleles 81343

Gene analysis for the protein phosphatase 2 regulatory subunit Bbeta checks for unusual variations in your genes. This helps to identify potential health issues related to these genes. It's a simple, non-invasive test using a blood or saliva sample.

185 services185 patients

Gene analysis (ataxin 7) for abnormal alleles 81181

Gene analysis for ataxin 7 involves studying your DNA to identify any unusual changes in the ataxin 7 gene. These changes, known as abnormal alleles, can cause health conditions like spinocerebellar ataxia. The test helps in early detection and management.

183 services183 patients

Gene analysis (cystatin b) of full sequence 81189

Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.

176 services176 patients

Gene analysis (hemochromatosis) common variants 81256

Gene 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.

176 services176 patients

Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants 81291

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.

176 services176 patients

Gene analysis (partner and localizer of brca2) targeted sequence analysis 81309

Gene 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.

176 services176 patients

Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants 81250

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.

137 services137 patients

Gene analysis (janus kinase 2) targeted sequence analysis 81279

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.

137 services137 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 81339

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.

137 services137 patients

Gene analysis (fanconi anemia, complementation group c) common variant 81242

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.

136 services136 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis 81298

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.

136 services136 patients

Gene analysis (partner and localizer of brca2) full sequence analysis 81307

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.

136 services136 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis 81317

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.

136 services136 patients

Gene analysis (bloom syndrome, recq helicase-like) 81209

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.

135 services135 patients

Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis 81249

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.

135 services135 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence 81223

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.

129 services129 patients

Gene analysis (coagulation factor ix) full sequence analysis 81238

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.

129 services129 patients

Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants 81226

Gene 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.

71 services71 patients

Frequently Asked Questions NPPES & CMS

Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.

What is Prism Molecular LLC's NPI number?

The NPI number for Prism Molecular LLC is 1558067199. It was assigned to this organization in the NPPES registry on February 6, 2023.

Where is Prism Molecular LLC located?

Prism Molecular LLC is located at 1801 Main St Ste 104, Blakely, PA 18447. The listed phone number is (570) 382-8125.

What is Prism Molecular LLC's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

When was this NPI record last updated?

The NPPES record for Prism Molecular LLC was last updated on April 1, 2024. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 2 years ago. If this record has changed at CMS more recently, you can request an on-demand re-check against the live CMS registry, directly from this page.