Allergies

46

427

244

Allergic diseases are complex genetic diseases resulting from the effect of multiple genetic and interacting environmental factors on pathophysiology. In recent years, considerable progress has been made in uncovering the contribution of these factors to an individual’s susceptibility to subsequent development and disease severity. The Allergy Panel assesses more than 40 related conditions by analyzing more than 240 genes and over 400 genetic markers.

Autism Spectrum Disorder

298

4682

1468

Autism spectrum disorder is being increasingly researched by doctors and scientists worldwide. Given the increase in cases of autism identified in different populations, we created this panel that allows doctors and parents to know more about this disorder and how to work with the genetic variants that influence different aspects of the individual’s health clearly and objectively. This panel analyzes 298 conditions, 1468 genes, and 4682 genetic variants.

Autoimmune

153

1888

613

Rheumatoid arthritis and SLE, along with a variety of other diseases, such as scleroderma, Sjögren’s syndrome, thyroid disorders, multiple sclerosis, and juvenile diabetes mellitus, belong to this group of autoimmune diseases. Often, multiple and different autoimmune diseases are seen in the same families. The Autoimmune Disease Panel assesses more than 120 related conditions, analyzing more than 540 genes and over 1150 markers.

Baby Test

370

7708

664

Through a simple collection of cheek cells, it is possible to assess 370 conditions in the baby. This test is important because it shows the genetic susceptibility to syndromes, allowing the health professional to have a broad view of the baby’s health and thus request, if necessary, other genetic tests. We know that the sooner syndromes and diseases are detected, the better the baby’s health prognosis, as treatments can be done in time.

Breast Cancer

21

370

178

A risk factor is something that increases your chances of getting a disease, like breast cancer. The BRCA1 and BRCA2 Genes: The most common cause of hereditary breast cancer is an inherited BRCA1 or BRCA2 gene mutation. In normal cells, these genes help to produce proteins that repair damaged DNA. Mutated versions of these genes can lead to abnormal cell growth, which can lead to cancer. Our Breast Cancer Panel assesses the risk factors in your genetic makeup.

Cancer

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1062

518

Cancer is a genetic disease – cancer is caused by certain changes in the genes that control the functioning of our cells, especially as they grow and divide. Genetic changes that promote cancer can be inherited from our parents if the changes are present in the germ cells. Genetic changes that cause cancer can also be acquired throughout life as a result of errors that occur when cells divide or exposure to cancer-causing substances that damage DNA. The Neoplasm Panel gathers risk susceptibility information genetics in more than 70 oncology-related conditions. More than 500 genes and more than 1,000 markers are analyzed from each individual and specified in detail with their risk score.

Cardiovascular

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1508

758

Cardiovascular diseases are the most deadly worldwide. Genetic analysis allows you to know in advance what the susceptibilities each person has for various diseases of the cardiovascular system. By identifying risks in advance, it is possible to initiate preventive measures. Our test analyses 115 cardiovascular-related conditions susceptibility by evaluating more than 750 genes.

Coronavirus-19

34

644

322

Coronavirus disease has changed the world, and research shows that genetics is a determining factor in the susceptibility of some people to contracting the virus more easily than others. Likewise, other details also have a genetic relationship, such as the tendency of COVID-19 to be severe and the development of Cytokine Storm, which has been a major cause of death from this virus. The Coronavirus-19 susceptibility test allows the patient and the doctor to understand the degree of risk and thus initiate the necessary protective measures for each type of result through analysis of 34 conditions and 644 genetic markers.

Diabetes

33

662

373

The Diabetes panel provides information on the risks of developing diabetes and deep information on the diabetes cause mechanisms, including cellular receptors.

Endocrinology and Hormones

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1140

The human body is made up of organs and glands responsible for the production of various hormones that regulate its functioning. Hormonal imbalances can result in various disorders and even cause serious illnesses, such as diabetes. This panel presents details of the functioning of the endocrine system through DNA analysis. Through an in-depth analysis of genetic variants, it is possible to identify in advance disorders that are often not present in biochemical tests.

Fertility

40

237

110

Increasingly, cases of infertility among individuals of both sexes are on the rise. This panel demonstrates each person’s susceptibilities to this disorder, thus enabling the most appropriate treatment.

Gastrointestinal Disease

86

1013

416

Many diseases involving the gastrointestinal organs are inherited or have a genetic predisposition involved in the expression of the disease. This information allows health professionals to adapt therapies and individually improve their results and quality of life. The Gastrointestinal Disease Panel assesses susceptibility to more than 80 conditions, analyzing over 400 genes and over 1000 genetic markers.

Genetics Disorders

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346

This panel demonstrates susceptibility to major genetic disorders, being an important research tool for doctors. More detailed research can be requested through this analysis to identify mutations that confirm susceptibility.

Gynecology

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1468

741

Gynecologists, obstetricians, and other health professionals increasingly incorporate genetics and genetic testing into medical practice. The correct interpretation of the genetic diagnostic test is highly dependent on an accurate clinical diagnosis, variants and prevalence of the disease, genetic heterogeneity, and phenotypic variability. As genetics becomes a more integral part of routine medical practice, obstetricians, gynecologists, and other health professionals are increasingly aware of advances in understanding genetic diseases and the fundamental principles of genetic screening. The Gynecology and Obstetrics Panel assesses more than 79 conditions, more than 740 genes, and over 1460 genetic markers.

Hematology

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390

Hematology is a branch of internal medicine that deals with the physiology, pathology, etiology, diagnosis, treatment, prognosis, and prevention of blood-related diseases. Although hematologists work with specialists from various medical and surgical specialties, hematology is more often linked to oncology. Hematologists and oncologists work together to care for adults and children with blood and bone marrow cancer, including leukemia and lymphoma. The Hematology Panel includes more than 150 conditions and parameters, analyzing more than 1900 markers and over 380 genes.

Inflammations

33

622

316

Inflammation is being increasingly studied and is related to several autoimmune diseases. Genetics combined with food has a great influence on the trigger of inflammation, which in turn can cause joint problems, such as arthritis, but also diseases such as Alzheimer’s and cardiovascular diseases. This panel lets you know in depth how your body works in relation to inflammations and what foods to avoid or supplement for a healthier life.

Men’s Health

68

1282

657

The Man’s Health provides a summary of genetic susceptibilities in 11 categories. It analyzes over 60 conditions over 1200 genetic markers in more than 650 genes. This is an excellent starting point.

Neurodegenerative

86

1862

552

One of the biggest problems today is the increase in neurodegenerative diseases, such as Parkinson’s disease and Alzheimer’s. Several factors, including genetics, contribute to the development of these and other neurodegenerative diseases. The analysis of the genes allows us to identify which individuals have greater or lesser susceptibility to their development and thus gives health professionals fundamental details on adopting essential preventive measures.

Nutrition

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1071

The Functional Nutrition Panel deeply analyzes the individual characteristics that influence diets. People are unique and, therefore, show different results when eating certain foods, such as fats, proteins, and carbohydrates. The Nutrition Panel demonstrates how genetics individually influence the response to different foods and why some people are more likely to put on weight than others. This panel also provides recommendations on what to avoid. This panel is the first step to getting to know your body and being able to adopt an effective diet to achieve your goals.

Oncology

78

712

271

Oncology is a genetic disease – cancer is caused by certain changes in the genes that control the functioning of our cells, especially as they grow and divide. Genetic changes that promote cancer can be inherited from our parents if the changes are present in the germ cells. Genetic changes that cause cancer can also be acquired throughout life as a result of errors that occur when cells divide or exposure to cancer-causing substances that damage DNA. The Neoplasm Panel gathers risk susceptibility information genetics in more than 70 oncology-related conditions. Each individual analyzed more than 270 genes and more than 700 markers, and their risk score is specified in detail.

Orthopedics and Rheumatology

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491

252

Many forms of rheumatic diseases, including forms of arthritis, have a genetic basis. Recent studies have revealed that several autoimmune diseases have a similar genetic basis. Many forms of arthritis are thought to be multifactorial and polygenic. Rheumatoid arthritis, a multifactorial disease, is a common type of inflammatory arthritis that affects many joints and occurs in approximately 1% of the population worldwide. The Orthopedics and Rheumatology Panel assesses more than 110 conditions related to orthopedics and rheumatology, analyzing more than 250 genes and over 490 genetic markers.

Pediatric and Genetic Diseases

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883

This panel is an essential tool for healthcare professionals and parents of pediatric patients. Knowing the susceptibilities makes it possible to start early treatments and thus avoid the manifestation of diseases.

Prostate

7

217

99

When prostate cancer is related to inherited genetic changes, the risk of cancer inherited depends on the gene involved. For example, mutations in the BRCA1, BRCA2, and HOXB13 genes are inherited in an autosomal dominant pattern, which means that one copy of the altered gene in each cell is sufficient to increase a person’s chance of developing cancer. Not all people who inherit mutations in these genes will develop cancer. The Prostate Cancer Panel assesses over 90 genes and more than 200 markers in 7 related conditions.

Vitamins, Minerals, and Antioxidants

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1612

849

Each individual metabolizes nutrients differently. This means that the need for vitamins, minerals, and antioxidants is also different among people. This panel shows the needs of each person from the genetic point of view, clearly identifying the needs and thus facilitating supplementation. It is important to compare some nutrients with the biochemical exam to understand the need for supplementation at the present moment.

Women’s Health

107

1811

805

The Woman’s Health provides a summary of genetic susceptibilities in 12 categories. This is an excellent starting point. It analyzes over 100 conditions, over 1800 genetic markers, and over 800 genes.