ELIXIR DIAGNOSTICS, LLC
NPI 1932843836
Clinical Medical Laboratory in Houston, TX

Q: What is Elixir Diagnostics, LLC's NPI number?

The NPI number for Elixir Diagnostics, LLC is 1932843836. It was assigned to this organization in the NPPES registry on April 26, 2022.

Q: What is Elixir Diagnostics, LLC's specialty?

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

Active since April 26, 2022CLIA 45D2257672 · Accreditation

17115 RED OAK DR STE 123, HOUSTON, TX 77090(979) 487-8258(832) 413-0059 Get Directions Write a Review

NPPES record last updated: April 26, 2022. Verified against the NPPES registry weekly; last sync: August 16, 2026.

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About Elixir Diagnostics, Llc NPPES

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

ELIXIR DIAGNOSTICS, LLC (NPI 1932843836) is a healthcare organization registered as a clinical medical laboratory in Houston, Texas and active in the NPI registry since April 2022. The organization holds an CLIA Accreditation certificate valid through April 24, 2027 and lists Ali Siddiqui, Owner, as its authorized official.

NPPES Registry Identity

NPI1932843836

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameELIXIR DIAGNOSTICS, LLC

Location Address17115 RED OAK DR STE 123Houston, TX 77090-2607

Mailing Address17115 Red Oak Dr Ste 123Houston, TX 77090-2607 · (979) 487-8258 · Fax (832) 413-0059

Phone(979) 487-8258

Fax(832) 413-0059

Organization SubpartNo

Authorized OfficialAli SiddiquiOwner · (561) 635-0392

Enumeration DateApril 26, 2022

NPPES CertifiedApril 26, 2022

✔ NPI 1932843836 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.

17115 RED OAK DR STE 123, Houston, TX 77090

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CLIA Laboratory Certificates CMS CLIA

Laboratory certificates issued under the Clinical Laboratory Improvement Amendments (CLIA) program, which sets federal quality standards for human laboratory testing in the United States. There is no official CMS crosswalk between CLIA and NPI numbers; these certificates are associated with this NPI by matching facility names, locations and phone numbers in the CMS CLIA registry.

Certificate of Accreditation 45D2257672

Elixir Diagnostics LLC · Houston, TX

Active · expires Apr 24, 2027

CLIA Number45D2257672

Laboratory TypeIndependent

Certificate Effective DateApril 25, 2025

Certificate Expiration DateApril 24, 2027

Laboratory DirectorDr. Kerollos A. Shaker

Laboratory Phone(561) 635-0392

Laboratory LocationElixir Diagnostics LLC17115 Red Oak Dr Suite 123, Houston, TX 77090

CLIA data matches this NPI record on: Address Name Phone

This is a certificate that is issued to a laboratory on the basis of the laboratory's accreditation by an accreditation organization approved by CMS.

Areas of Expertise CMS Part B claims 45

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.

Molecular pathology procedure level 1 81400

A 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.

934 services465 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.

654 services654 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.

412 services411 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.

402 services402 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.

400 services400 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.

374 services374 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.

372 services372 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.

369 services368 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.

359 services358 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.

337 services337 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.

334 services334 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.

334 services334 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.

333 services332 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.

333 services333 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.

329 services329 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.

311 services311 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.

305 services305 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.

298 services298 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.

298 services298 patients

Gene analysis (solute carrier organic anion transporter family, member 1b1) for common variant 81328

Gene 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.

292 services292 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.

289 services287 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.

289 services287 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.

285 services285 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.

284 services284 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.

282 services282 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.

282 services282 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.

282 services282 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.

282 services282 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.

282 services282 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.

279 services279 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.

276 services276 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.

275 services275 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.

275 services275 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.

266 services266 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 9) common variants 81227

Gene 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.

223 services223 patients

Gene analysis (sphingomyelin phosphodiesterase 1, acid lysosomal) common variants 81330

Gene analysis of sphingomyelin phosphodiesterase 1, acid lysosomal, involves studying specific variants in your genes. This helps understand your body's enzyme production, which can influence health conditions. It's a non-invasive procedure using a simple blood or saliva sample.

207 services207 patients

Gene analysis (serpin peptidase inhibitor, clade a, alpha-1 antiproteinase, antitrypsin, member 1) common variants 81332

Gene analysis for SERPINA1 common variants is a test that checks for changes in the SERPINA1 gene. This gene helps protect your lungs and liver from damage. Certain changes can lead to conditions like lung disease or liver problems. This test helps identify those changes.

204 services204 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.

167 services167 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.

166 services166 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants 81225

Gene 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.

134 services134 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.

56 services56 patients

Gene analysis (transforming growth factor beta-induced) for common variants 81333

Gene analysis for common variants in the transforming growth factor beta-induced (TGFBI) gene helps understand your genetic makeup better. This procedure checks for variations in the TGFBI gene, which can influence your health. It's a safe, non-invasive test that uses a simple blood or saliva sample.

25 services25 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.

19 services19 patients

Gene analysis (nudix hydrolase 15) for common variants 81306

Gene analysis for Nudix Hydrolase 15 common variants is a genetic test that identifies changes in your NUDT15 gene. These changes can affect how your body responds to certain medications, helping your healthcare provider to personalize your treatment plan.

15 services15 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.

11 services11 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 Elixir Diagnostics, LLC's NPI number?

The NPI number for Elixir Diagnostics, LLC is 1932843836. It was assigned to this organization in the NPPES registry on April 26, 2022.

Where is Elixir Diagnostics, LLC located?

Elixir Diagnostics, LLC is located at 17115 Red Oak Dr Ste 123, Houston, TX 77090. The listed phone number is (979) 487-8258.

What is Elixir Diagnostics, LLC's specialty?

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

Does Elixir Diagnostics, LLC hold a CLIA laboratory certificate?

Yes. A Certificate of Accreditation (number 45D2257672) is associated with this NPI, valid through April 24, 2027. CLIA certificates authorize laboratory testing under the federal Clinical Laboratory Improvement Amendments program.

When was this NPI record last updated?

The NPPES record for Elixir Diagnostics, LLC was last updated on April 26, 2022. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 4 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.

About Elixir Diagnostics, Llc NPPES

NPPES Registry Identity

Specialties & Licenses

CLIA Laboratory Certificates CMS CLIA

Certificate of Accreditation · 45D2257672

Areas of Expertise CMS Part B claims 45

Frequently Asked Questions NPPES & CMS

What is Elixir Diagnostics, LLC's NPI number?

Where is Elixir Diagnostics, LLC located?

What is Elixir Diagnostics, LLC's specialty?

Does Elixir Diagnostics, LLC hold a CLIA laboratory certificate?

When was this NPI record last updated?

Certificate of Accreditation 45D2257672