Official registry information on file with the National Plan and Provider Enumeration System.
UNITY HOLDING GROUPS LLC (NPI 1023720778) is a healthcare organization registered as a clinical medical laboratory in Jessup, Pennsylvania and active in the NPI registry since December 2022. The organization lists Kenneth Oconnor, Owner, as its authorized official.
NPPES Registry Identity
NPI1023720778
Entity TypeOrganization
Primary Taxonomy291U00000X
Legal Business NameUNITY HOLDING GROUPS LLC
Location Address1 ALBERIGI DR STE 109Jessup, PA 18434-1831
Mailing Address900 N Federal Hwy Ste 450Boca Raton, FL 33432-2755 · (561) 810-0610
(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.
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.
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.
3,395 services3,395 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.
3,140 services3,140 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.
3,139 services3,139 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.
3,131 services3,131 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.
3,126 services3,126 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.
3,125 services3,125 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.
3,121 services3,121 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.
3,063 services3,063 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.
3,031 services3,031 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.
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.
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.
2,797 services2,797 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.
2,668 services2,668 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.
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.
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.
2,560 services2,560 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.
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.
2,515 services2,515 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.
2,502 services2,502 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.
2,501 services2,501 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.
2,500 services2,500 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.
2,499 services2,499 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.
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.
2,499 services2,499 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.
2,497 services2,497 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.
2,495 services2,495 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.
2,491 services2,491 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.
2,487 services2,487 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.
2,329 services2,329 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.
2,327 services2,327 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.
2,323 services2,323 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.
2,264 services2,264 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.
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.
1,944 services1,944 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.
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.
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.
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.
1,877 services1,877 patients
Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis 81295
Gene 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.
886 services886 patients
Gene analysis (adenomatous polyposis coli), full gene sequence 81201
Gene 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.
881 services881 patients
Gene analysis (hemoglobin, subunit beta) full sequence analysis 81364
Gene analysis of hemoglobin, subunit beta, is a detailed examination of a specific gene in your body. This test helps identify any changes or mutations that may lead to health conditions, such as blood disorders. It's a non-invasive procedure and a vital tool in personalized medicine.
819 services819 patients
Gene analysis (methyl cpg binding protein 2) full sequence analysis 81302
Gene analysis, specifically Methyl CpG Binding Protein 2 (MECP2) full sequence analysis, is a detailed examination of your DNA. This test focuses on the MECP2 gene, which plays a crucial role in nerve cell function and development. The results can help identify alterations or mutations that may cause certain health conditions.
816 services816 patients
Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence 81185
Gene analysis of the calcium voltage-gated channel subunit alpha1 a involves examining your DNA to understand how your body regulates calcium. This helps identify potential health risks related to calcium imbalances. It's a non-invasive procedure involving a simple blood or saliva sample.
810 services810 patients
Gene analysis (survival of motor neuron 1, telomeric) for dosage/deletion 81329
Gene analysis for survival of motor neuron 1 (SMN1) involves studying your DNA to identify changes or deletions in the SMN1 gene. This gene plays a key role in motor neuron health. Alterations can lead to conditions like spinal muscular atrophy. The process is safe and non-invasive.
726 services726 patients
Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants 81162
Gene 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.
393 services393 patients
Gene analysis (mpl proto-oncogene, thrombopoietin receptor) for detection of common variants 81338
Gene analysis for the MPL proto-oncogene, thrombopoietin receptor, is a test that looks for common genetic variants. This helps in understanding certain health conditions related to blood cell production. It's a non-invasive procedure, involving a simple blood draw.
274 services274 patients
Gene analysis (phosphatase and tensin homolog), full sequence analysis 81321
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.
184 services184 patients
Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis 81292
Gene 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.
116 services116 patients
Gene analysis (breast cancer 2) of full sequence 81216
Gene analysis (breast cancer 2) of full sequence is a test that studies your DNA to identify any changes or mutations in the genes associated with an increased risk of certain types of cancer.
51 services51 patients
Gene analysis (phospholipase c gamma 2) for common variants 81320
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.
43 services43 patients
Gene analysis for cancer (neuroblastoma) 81311
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.
30 services30 patients
Gene analysis (dihydropyrimidine dehydrogenase) for common variant 81232
Gene analysis for dihydropyrimidine dehydrogenase (DPD) common variant involves studying a specific gene in your body. This gene affects how your body processes certain medications. The test identifies any changes in this gene which may influence your response to these medications.
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.
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.
24 services24 patients
Gene analysis (additional sex combs like 1, transcriptional regulator) full sequence analysis 81175
Gene analysis, specifically of the Additional Sex Combs Like 1, is a process where your DNA is examined to identify changes or alterations in a particular gene. This analysis helps to understand certain health conditions better and can guide treatment decisions.
23 services23 patients
Gene analysis (enhancer of zeste 2 polycomb repressive complex 2 subunit) of full sequence 81236
Gene analysis of the full sequence of the Enhancer of Zeste 2 Polycomb Repressive Complex 2 Subunit (EZH2) involves examining this specific gene in detail. This gene plays a crucial role in cell growth and division. The analysis helps identify any mutations that could potentially lead to health issues.
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.
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.
21 services21 patients
Gene analysis (ccaat/enhancer binding protein [c/ebp], alpha) full gene sequence 81218
Gene analysis of the CCAAT/Enhancer Binding Protein (C/EBP), Alpha, involves studying the entire sequence of this particular gene. This can help identify variations or changes in the gene that might affect your health. This process is done in a lab using a sample of your cells.
11 services11 patients
Gene analysis (tumor protein 53) full sequence analysis 81351
Gene analysis, specifically tumor protein 53 (TP53) full sequence analysis, is a test that examines the entire TP53 gene. This gene plays a key role in preventing cancer. If there are changes or mutations in this gene, it could lead to an increased risk of developing various types of cancer.
11 services11 patients
Other Providers at the Same Location NPPES2
Providers registered at the same practice address, or within the immediate area, according to the NPPES registry.
Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.
What is Unity Holding Groups LLC's NPI number?
The NPI number for Unity Holding Groups LLC is 1023720778. It was assigned to this organization in the NPPES registry on December 14, 2022.
Where is Unity Holding Groups LLC located?
Unity Holding Groups LLC is located at 1 Alberigi Dr Ste 109, Jessup, PA 18434. The listed phone number is (561) 810-0610.
What is Unity Holding Groups 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 Unity Holding Groups LLC was last updated on May 16, 2023. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 3 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.
# Unity Holding Groups Llc · NPI 1023720778
Clinical Medical Laboratory organization in Jessup, Pennsylvania. Organization record, active in the CMS NPPES registry since December 14, 2022.
## Identity
- **NPI:** 1023720778 (Entity type: Organization)
- **Enumerated:** December 14, 2022
- **Primary specialty:** Clinical Medical Laboratory · taxonomy 291U00000X
- **Organization subpart:** No
- **Authorized official:** Kenneth Oconnor, OWNER
## Practice location
- **Address:** 1 ALBERIGI DR STE 109, Jessup, PA 18434-1831
- **Phone:** (561) 810-0610
## Record status
- **NPPES last updated:** May 16, 2023
---
Source: [NPI Profile](https://npiprofile.com/npi/1023720778) · Data from the CMS NPPES public registry.
# Unity Holding Groups Llc · NPI 1023720778
Clinical Medical Laboratory organization in Jessup, Pennsylvania. Organization record, active in the CMS NPPES registry since December 14, 2022.
## Identity
- **NPI:** 1023720778 (Entity type: Organization)
- **Enumerated:** December 14, 2022
- **Primary specialty:** Clinical Medical Laboratory · taxonomy 291U00000X
- **Organization subpart:** No
- **Authorized official:** Kenneth Oconnor, OWNER
## Practice location
- **Address:** 1 ALBERIGI DR STE 109, Jessup, PA 18434-1831
- **Phone:** (561) 810-0610
## Record status
- **NPPES last updated:** May 16, 2023
---
Source: [NPI Profile](https://npiprofile.com/npi/1023720778) · Data from the CMS NPPES public registry.