Conditions

At Genome It All, we cover a vast amount of different conditions. Our reporting if very extensive and unique to each customer. We do this so that our customers can find the answers they need, specific to them.

What you can expect to see on your report:

  • Allergies- Susceptibilities, triggers

    • Bugs, Dust mites, Food, Gluten, Lactose, Seasonal

  • Aging- Susceptibilities, Traits on aging, Longevity

  • Amino Acids- Changes, Deficiencies, Breakdown abilities

    • 2-aminobutyrate (AABA), Alanine (Ala), Arginine (Arg), Citrulline (Cit), Creatine (CK), Cysteine (Cys), Glutaric aciduria, Glutamine (Glu), Glycine (Gly), Isobutyryl-CoA dehydrogenase (IBD), Isoleucine (Ile), Acetyl L-Carnitine (LCT), Leucine (Leu), Lysine (Lys), Methionine (Met), Ornithine, Proline (Pro), Serine, Tryptophan, Tyrosine, Valine (Val).

  • Antibody- Response, Susceptibilities

    • Antineutrophil Cytoplasmic Antibodies (ANCA), Cytokines, Duffy, Insulin-like Growth Factor, Neutrophils, Immunoglobulin: A, D, E, G.

  • Antioxidant- Abilities, Cellular, Production, Recycling

    • COQ10, Glutathione, Indole propionic

  • Athletic Potential- Muscle types, Response to fitness, Aerobic capacity, Endurance, Strength.

    • Angiotensin, Metabolic Equivalent Task (MET), VO2 Max.

    • Glycogen storage disease.

  • Autoimmune -Reactions, Risks, Susceptibilities

    • Interleukin-6 (ILG), Tumor Necrosis Factor (TNF)

    • Arteriosclerosis, Bechet's, Myasthenia Gravis, Multiple sclerosis, Pediatric, Rheumatoid arthritis, Sjogren's, Systemic lupus erythematosus, Systemic sclerosis

  • Birth defects- Risks, Carrier status

    • Conotruncal Heart Defects, Microcephaly, Neural tube defects (NTDs), Smith-Lemli-Opitz syndrome.

  • Blood- Types, Changes, Risks, Coagulation.

    • Albumin, Antithrombotic, Citrate, Complement C3, D-dimer, Ferritin, Fibrin, Hematocrit, Hemoglobin, Mean Corpuscular Hemoglobin (MCH), Mean corpuscular volume (MCV), Plasminogen, Platelet, Porphyrin, Pressure, Proteins, Prothrombin, Thromboplastin.

    • Beta thalassemia, Factor IX deficiency disease (Hemophilia B), Factor V, Upshaw-Schulman syndrome (USS), Von Willebrand factor (VWF), X-linked sideroblastic anemia.

  • Blood Pressure- Preeclampsia, Sensitivities, Risks, Heritable Traits

    • Diastolic, Mean Arterial, Systolic, Pulse/heart rate.

  • Brain- Activity, Changes, Development, Structure, Risks, Traits, Volume

    • Amygdala, Atrophy, Carotid intima media thickness, Cerebral cortex, Cerebrospinal fluid (CSF), Entorhinal cortex, Grey Matter, Hippocampus, White Matter.

    • Aicardi-goutieres syndrome, Aneurysm, Cerebral infarction, Congenital muscular dystrophy, Craniopharyngioma, Encephalopathy, Glioma, Heterotopia, Hereditary diffuse leukoencephalopathy with spheroids, Hippocampal sclerosis of aging, Holoprosencephaly, Intracerebral hemorrhage, Lissencephaly, Palsy, Pigmented nodular adrenocortical disease, Polymicrogyria, Scaphocephaly, Traumatic brain injury (TBI), X-linked adrenoleukodystrophy.

  • Cancer- Risks, Susceptibilities, Traits, Toxin exposure changes, Benefits

    • Basal, Bladder, Blood, Brain, Digestive, Kidney, Lung, Mouth, Neoplasm, Thyroid.

    • Adenoma, B-Cell Non-Hodgkin Lymphoma, Bloom syndrome, Breast, Chronic myelomonocytic leukemia (CMML), Endocrine, Endometrial, Esophageal squamous-cell carcinomas, Ewing sarcoma, Familial adenomatous polyposis, Follicular lymphoma, Gallbladder, Glioma, Glioblastoma, Hamartoma, Hereditary hemorrhagic telangiectasia, Juvenile polyposis syndrome, Leukemia, Lymphoma, Lynch Syndrome, Melanoma, Meningioma, Mesothelioma, Multiple endocrine neoplasia, Myeloma, Myeloproliferative Neoplasms, Nasopharyngeal carcinoma, Neuroblastoma, Neurofibromatosis, Non-hodgkins Lymphoma, Non-small cell lung cancer, Pancreatic cancer, Prostate cancer, Renal cell carcinoma, Retinoblastoma, Sarcoma, Squamous cell carcinoma, Squamous intraepithelial neoplasia.

  • Cardiovascular -Health, Risks, Traits, Susceptibilities

    • Arrhythmia, Atrial septal defect, Brain natriuretic peptide (BNP), Electrocardiogram (ECG), PR interval, QRS wave, QT interval, Rate, Rhythm.

    • Acute coronary syndrome, Acute myocardial infarction, Atrial fibrillation, Becker muscular dystrophy (BMD), Brugada syndrome (BS), Cantú syndrome, Cardiac arrest, Congestive heart failure, Coronary calcification, Duchenne muscular dystrophy, Hypertension, Hypertrophic cardiomyopathy, Long QT syndrome, Myocardial infarction, Tachycardia, Ventricular septal defect.

  • Cells -cellular damage by free radicals, cell traits/variations.

    • B lymphocyte, Fetal hemoglobin, Kupffer, Leydig, Macrophages, T lymphocytes, Red blood cells, White blood cells/ Eosinophil.

    • Graft-versus-host disease, Niemann Pick Disease C1, Sarcoidosis, Sickle, Stem.

  • Chemicals- Toxins

    • Benzalkonium chloride, Ethanol, Phosphate, Polyvinyl chloride, Trimethylamine

  • Cholesterol- Build up potential, Traits, Risks

    • High-density lipoprotein (HDL), Lecithin-cholesterol acyltransferase (LCAT), Low-density lipoprotein (LDL), Total, Triglycerides.

    • Familial hypercholeserolemia,

  • Chromosomes- Abnormalities, Structure and Function

    • Telomeres, Y chromosome.

    • Nijmegen breakage syndrome (NBS).

  • Defects -Skeletal, Developmental, Risks, Carrier status

    • Cleft Lip Palate, Contruncal heart defects, Frontonasal dysplasia, Hypospadias, Morphology, Tetralogy of fallot, Ventricular septal defect (VSD)

  • Deficiency-

    • Acetyl-CoA acetyltransferase, Adenylosuccinate lyase, Argininosuccinate lyase deficiency, Aromatase, Biotinidase, Tetrahydrobiopterin, Glutaric aciduria, Methylmalonyl-CoA epimerase deficiency, Phosphorylation, Short-chain acyl-CoA dehydrogenase.

  • Degeneration- Degenerative disc disease, Risks

  • Dementia- Risks

    • Alzheimer’s Disease, Frontotemporal, Lewy body disease.

  • Dental- Susceptibilities, Deficiencies

    • Agenesis, Caries, Gums, Enamel.

    • Odontogenesis, Periodontitis, Temporomandibular joint dysfunction

  • Development- Growth, Height

    • Idiopathic short stature, Small for gestational age

  • Developmental disorder- Risks, Carrier status

    • Craniofacial.

    • Adolescent idiopathic scoliosis, Arthrogryposis multiplex congenita, Asperger's, Autism, Bardet-Biedl syndrome, Beckwith-Wiedemann syndrome, Cornelia de Lange syndrome, CHARGE syndrome, Charcot-Marie-Tooth disease, Chondrodysplasia, Cockayne syndrome, Coffin-Siris syndrome, Costello syndrome, Crouzon syndrome, Geleophysic dysplasia, Hemophagocytic lymphohistiocytosis, Kallmann syndrome, Lethal congenital contracture syndrome, Limb-girdle muscular dystrophy, Levy-Hollister syndrome, Multiple congenital anomalies-hypotonia-seizures syndrome, Metaphyseal dysplasia, Spahr type, McKusick Kaufman syndrome, Microcephaly, Microphthalmia, Mucolipidosis, Mucopolysaccharidosis, Mowat-Wilson, N-terminal acetyltransferase deficiency, Multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS), Myhre syndrome, N-terminal acetyltransferase deficiency, Osteoglophonic dysplasia, Pfeiffer syndrome, Phosphoglycerate dehydrogenase deficiency, Pitt-Hopkins syndrome, Roberts-SC phocomelia syndrome, Rett syndrome, Rhizomelic chondrodysplasia punctata, Roberts-SC phocomelia syndrome, Rubinstein-Taybi syndrome, SHORT syndrome, Spondyloepimetaphyseal dysplasia Missouri type, Smith-Kingsmore syndrome, Seckel syndrome, Tatton-Brown-rahman syndrome, Tay-Sachs disease, Visceral heterotaxy.

  • Dietary-

    • Additives, Bitter, Carbs.

    • Asparagus, Sodium, Sugar, Vegetables.

  • Digestive- Food sensitivities, Digestive problems, Risks

    • Crohn’s disease, Dysbiosis, Gastroesophageal reflux disease, Gastritis, Helicobacter pylori, Hereditary fructosuria, Hypochlorhydria, Intestinal atresia, Irritable Bowel disease, Microbiota, Pancreatitis, Parasitic Infections, Slow transit constipation, Stomach acid, Ulcerative Colitis

  • Disorders- Developments, Mental, Growing, Aging, Risks, Carrier status

    • Dystonia, Eating, Hair, Migraine, Movement, Neuromuscular.

    • Bardet–Biedl syndrome, Brachydactyly, Congenital ichthyosis, Cutis laxa, Creutzfeldt-Jakob disease, Congenital adrenal hyperplasia, Congenital disorder of glycosylation, Congenital disorder of glycosylation type, Coffin-Siris syndrome, Costello syndrome, Diffuse mesangial sclerosis, Friedreich's ataxia, Familial dyskinesia with facial myokymia, Glutaric acidemia, Ghosal hematodiaphyseal, Huntington disease, Hermansky-Pudlak, Hirschsprung disease, Joubert syndrome, Limb-girdle muscular dystrophy, dystroglycanopathy, Lipodystrophy, Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, Methylmalonic acidemia Noonan syndrome, Noonan- like syndrome with loose anagen hair, Papillon-Lefèvre syndrome, Pitt-Hopkins-like syndrome, Pseudoxanthoma elasticum, Reticulosis, Rhizomelic chondrodysplasia punctata, Rubinstein-Taybi syndrome, Spinocerebellar ataxia, Sjogren-Larsson syndrome, Telangiectasia, Tuberous Sclerosis Complex, Von Hippel-Lindau syndrome, Vogt-Koyanagi- Harada Disease, Wolfram.

  • Elements -Metals, Mineral levels or deficiencies

    • Copper, Iron, Lead, Mercury, Phosphorus, Sulfur

  • Endocrine- Pituitary

  • Environmental- Exposure, Reduced clearance or build up

    • 3-phenylpropionate hydro cinnamate, Aflatoxin B1, Carbon Monoxide, Chemicals, Cigarette smoke, Dioxins, Heterocyclic amines, Levulinate, Pesticides, Phthalates, Pigments, Polychlorinated biphenyls (PCBs), Radiation, Reactive oxygen species

  • Enzymes- Breakdown, Deficiencies, Risks

    • Alkaline phosphatase, Arylsulfatase A, Aspartate aminotransferase, Butyrylcholinesterase, Gamma glutamyl transpeptidase, Guanidinoacetate methyltransferase, Lactate Dehydrogenase, Matrix Metalloproteinase, NADPH (nicotinamide adenine dinucleotide phosphate), Phenyllactate, Plasmin, Xanthine.

    • Exocrine pancreatic insufficiency, Hereditary coproporphyria, Isovaleryl-CoA dehydrogenase deficiency, Glycogen storage disease, Metachromatic leukodystrophy (MLD).

  • ENT (Ear, nose, throat)- Development, Risks, Carrier status, Smelling ability

    • Motion, Smell, Tonsil, Vertigo

    • Rhinosinusitis, Usher syndrome

  • Eyes -Vision changes/Loss, Carrier status

    • Axial, Eye dystrophy, Color, Cornea, Cup, Defects, Disc, Optic disc, Pressure, Eye Refraction, Retina, Vision.

    • Age related macular degeneration, Astigmatism, Bette crystalline corneoretinal dystrophy, Cataracts, Glaucoma, Ocular albinism, Optic atrophy, Nearsightedness (myopia), Retinopathy

  • Fatty Acids- Aromatic, Metabolism

    • 2-hydroxyisobutyrate/ alpha-hydroxybutyrate, Arachidonic acid (Omega 6), Omega-3, Docosatrienoic acid, Eicosapentaenoic acid, Long-chain fatty acids, Palmitoleic acid, Phenyl acetate, Polyunsaturated fatty acids.

  • Female- Traits, Risks

    • Breasts, Disorders, Ovaries

    • Endometriosis, Fibroids, Ovarian dysgenesis, Ovarian hyperstimulation syndrome, Pelvic organ prolapse, Polycystic ovary syndrome (PCOS)

  • Genetic- Changes, Carrier status, Expression; DNA repair

    • Haplogroup, Transcription

    • Lethal arthrogryposis with anterior horn cell disease

  • General- Energy/Energy Production

  • Hearing- Loss, Risks, Carrier status

    • Hearing Impairment, Otosclerosis, Pili torti.

  • Hormones- Changes, Susceptibilities, Therapy

    • Adrenocorticotropic, Androgen, Cortisol, Dehydroepiandrosterone (DHEA), Epinephrine, Gonadotropin, Growth hormone, Leptin, Melatonin, Oestradiol, Oxytocin, Sex hormones.

  • Immune system- Ability, Reaction, Risks, Immunities

    • Histamine, Histidine

    • Ataxia, Autoimmune lymphoproliferative syndrome, Common variable immunodeficiency, Granulomas, Graves disease, Hyper IgM, Immunodeficiency, centromeric instability, and facial dysmorphism, Mannose-binding protein deficiency, Major histocompatibility complex, Severe Combined Immune Deficiency

  • Infant Disorders- Carrier status, Risks

    • Nervous system, Neurological, Respiratory.

    • Bifunctional peroxisomal enzyme deficiency, Canavan disease, Congenital amegakaryocytic thrombocytopenia, Ceroid lipofuscinosis neuronal, hypertrophic pyloric stenosis, Infantile hypertrophic pyloric stenosis, GM1-gangliosidosis, Mitochondrial complex III deficiency neonatal diabetes mellitus, NGLY1-congenital disorder of deglycosylation, Non-ketotic hyperglycinemia, Persistent hyperinsulinemic hypoglycemia of infancy, Sudden infant death syndrome, Tyrosinemia, Zellweger syndrome.

  • Infections- Susceptibilities/Risks.

    • Bacteria, Herpes, Leprosy, Septic.

  • Inflammation- Response to stimuli, Sensitivities, Triggers

    • galectin-3

    • Eosinophilic esophagitis (EoE), Erythrocyte sedimentation rate (ESR), Gout, Tumor Necrosis Factor (TNF), TNF receptor-associated periodic fever syndrome.

  • Insulin- Diabetes, Blood Sugar & Cardiovascular Markers

    • Fasting, Glucose, Insulin Secretion Index, HOMA-IR (Homeostatic Model Assessment for Insulin Resistance), Resistance, Sensitivity.

    • Diabetes, Hypoglycemia, Metabolic syndrome, MITCHELL-RILEY SYNDROME (MTCHRS), Type 1 diabetes nephropathy.

  • Kidney- Disorders, Risks, Defects, Function

    • Dialysis, Disease, Dysplasia, Filtration, Hematuria, Renin, Renal, Stones, Transplant

    • Acute Kidney Injury, Aquaporin 1 deficiency, Autosomal recessive distal renal tubular acidosis, Factor H deficiency, End-stage renal disease, Glomerulocystic kidney, Idiopathic membraneous nephropathy, Nephrotic syndrome, Nephropathy, Polycystic kidney disease, Primary hyperoxaluria, Renal Hypomagnesemia

  • Learning- Abilities, Benefits, Deficiencies, Traits

    • Dyslexia, Education, Speech

  • Lifestyle - Preference, Risk

    • Alcohol, Caffeine, Cannabis, Drugs, Gambling, Smoking,

  • Lipids- Structure and Function, Traits, Risks/Susceptibilities, Defect, Metabolism

    • Apolipoprotein, Apolipoprotein A-I (apo A-I), Apolipoprotein A-II (apo A-II), Lipoprotein(a), Phospholipid, Sphingolipid, Sulfatides.

    • Hyperlipoproteinemia, Sitosterolemia, Very long chain acyl-CoA dehydrogenase deficiency.

  • Liver- Disorders, Risks, Defects, Function

    • Bile, Bilirubin, Cholestasis, Cirrhosis, Dysplasia, Hepatocyte growth factor, Hepatotoxicity.

    • Acute intermittent porphyria, Alkaline phosphatase, Aspartate transaminase, Dubin-Johnson syndrome, Gamma-glutamyl transpeptidase, Gallstones, Hepatitis, Nonalcoholic fatty liver disease, Primary biliary cirrhosis, Primary sclerosing cholangitis.

  • Male- Traits, Risks

    • Prostate, Sex steroid.

    • Erectile dysfunction.

  • Mental Capacity- Mental abilities, Traits

    • Cognitive, IQ, Memory.

    • ATR-X syndrome, Mental retardation, Mental retardation-hypotonic facies syndrome, Poretti-boltshauser syndrome.

  • Mental Health - Risks/Susceptibilities

    • Aging, Neuroticism, Prion.

    • Attention deficit hyperactivity disorder (ADHD), Bipolar, Conduct Disorder, Obsessive compulsive disorder (OCD), Posttraumatic Stress Disorder (PTSD), Schizophrenia.

  • Metabolism- Fat & Carbohydrate Metabolism, Vitamins

    • Carnitine palmitoyltransferase, N-acetylcarnosine, X- 12095- -N1- methyl-3-pyridine-4- carboxamide.

    • Metabolic Syndrome, Maple syrup urine disease, Niemann-Pick disease.

  • Methylation- Pathways, Abilities, Deficiencies, Risks/Susceptibilities

    • CpG islands, Homocysteine.

    • Cystathioninuria.

  • Minerals- Levels, Absorption, Deficiencies, Reduced clearance, Build up

    • Calcium, Magnesium, Phosphorus, Potassium, Oxalic acid, Selenium

  • Mitochondria- Changes, Structure/Function, Risks/Susceptibilities

    • Adenosine triphosphate, Complex III.

    • Alpers, Leigh syndrome (LS).

  • Mood Disorder- Risks/Susceptibilities

    • Depression, seasonal affective disorder (SAD).

  • Musculoskeletal- Changes, Structure/Function, Risks/Susceptibilities, Disorders

    • Anterior cruciate ligament, Adenosine monophosphate deaminase, Lactic acid, Motion, Pain, Tendon, Tissue.

    • Emery-Dreifuss muscular dystrophy, Ehlers-Danlos syndrome, Fibromyalgia, Intermediate muscular dystrophy, Limb-girdle muscular dystrophy, Muscular atrophy, Muscular dystrophy, Myopathy, Myotonia, Paralysis, Systemic sclerosis.

  • Nervous system- Nerves, Changes, Structure/Function, Risks/Susceptibilities

    • Central Nervous system, Myelin, Polyglucosan, Psychomotor, Tumor.

    • Angelman, Carpal tunnel syndrome, Ceroid lipofuscinosis neuronal, Charcot-Marie-Tooth Neuropathy, Dysautonomia, Encephalopathy, familial, with neuroserpin inclusion bodies, Neuroma, Parkinson's, Salla disease, Spastic paraplegia, Tourettes.

  • Neurological -Risks/Susceptibilities

    • Neurocognition, Neurodegeneration, Neurodevelopmental, Neuropathy, Neuron Disease, Stroke, Tangles, Tremor, Tics.

    • Amyotrophic lateral sclerosis Acute hepatic porphyria, Alpha-methyl acyl-CoA racemase deficiency, Asparagine Synthetase Deficiency, Carbohydrate-deficient glycoprotein syndrome, Charcot-Marie-Tooth disease, Desmosterolosis, Dihydropyrimidine dehydrogenase deficiency, Epilepsy, Hereditary motor and sensory neuropathy, Mucolipidosis, Parkinson's, Restless legs syndrome (RLS), Seipinopathy, Silver spastic paraplegia syndrome, Temtamy

  • Neurotransmitter -Brain chemistry balance, Changes

    • 3-Methoxy-4-hydroxyphenylglycol (MHPG), Dopamine, GABA (gamma-aminobutyric acid), Serotonin.

  • Organisms-

    • Parasites, Worms.

  • Osteo- Bone Health, Softening, Traits, Breakdown, Carrier Status

    • Bone Marrow, Bone mineral density (BMD), Broad-band ultrasound attenuation (BUA), Degeneration, Development, Fractures, Ossification, Osteolysis, Sclerosteosis, Scoliosis, Thoracic Spine.

    • Ankylosing spondylitis, Arthritis, Metachondromatosis, Osteogenesis imperfecta (OI), Osteonecrosis of the femoral head (ONFH), Osteoporosis, Ossification of the posterior longitudinal ligament, Paget’s disease of bone, Spondylometaphyseal dysplasia with cone-rod dystrophy.

  • Oxidative-

    • Ammonia, Homovanillic acid (HVA).

    • Cytochrome c oxidase i deficiency.

  • Personality-

    • Agreeableness, Creativity, Leadership, Novelty, Openness, Persistence, Political

  • Pharmacogenomics- Reactions to medicines, Metabolism, Deficiencies, Reduced breakdown, Build up, Risks

  • Proteins- Structure/Function, Traits, Changes

    • Amyloid, β2-glycoprotein I (β2GPI), Complement C4, C-reactive protein (CRP), Collagen, Cystastin C, Galectin-3 (gal3), Glycoprotein, ICAM-1 (Intercellular Adhesion Molecule 1), Monoclonal, myeloperoxidase, Peptides, Perforin, soluble P-selectin, Soluble ST2 (sST2).

    • monoclonal gammopathy of unknown significance.

  • Psychological- Traits, Risks, Carrier status, Response to Stress

    • Anger, Anxiety, Coping, Emotion, Stress, Suicide, Tendency.

  • Reproduction- Ability to reproduce, Carrier status, Risks

    • Follicle-stimulating hormone (FSH), Gestation, Persistent organic pollutants (POPs), Placenta, Sperm.

    • Hypogonadism, Infertility, Menarche, Menopause, Miscarriage, Preeclampsia.

  • Respiratory- Risks, function

    • Cilia, Fluid, Forced expiratory volume, Forced vital capacity, Function, Lung, Mucus, Nitric oxide, Obstruction.

    • Acute respiratory distress syndrome, Asthma, Bronchopulmonary dysplasia, Bronchiectasis, Central hypoventilation, Chronic obstructive pulmonary disease, Cystic fibrosis (CF), Emphysema, Fibrosis, Hypertension, Invasive Pulmonary Aspergillosis, Pneumonia, Pulmonary Thromboembolism, Tuberculosis.

  • RNA -Structure/Function, Changes, Risks

    • Transfer ribonucleic acid (tRNA), Uracil.

  • Sensitivity-

    • Fear, Heat, Pain, Personality, Startle, Surgery, Temperature.

  • Skin- Traits, Risks/Susceptibilities, Disorders, Sensitivities, Quality

    • Acne, Advanced glycation end products, Cutis laxa, Elanocytic nevi (moles), Eczema, Melanin, Nevus, Psoriasis, Sun, Vitiligo.

    • Darier disease, Dermatitis, Dyskeratosis congenita, Ectodermal dysplasia, Epidermolysis bullosa, Fibrofolliculomas, Hypohidrotic X-linked ectodermal dysplasia, Palmoplantaris striata, Porphyria, Skin fragility woolly hair syndrome, Xeroderma pigmentosum.

  • Sleep- Sleeping patterns, Tendencies, Traits

    • Circadian Rhythm, Duration, Quality.

    • Insomnia, Narcolepsy.

  • Thyroid- Risks/Susceptibilities, Function

    • Parathyroid, Free T3, Free T4, Thyroid peroxidase, Thyroid-stimulating hormone (TSH), Volume.

    • Generalized thyroid hormone resistance, Goiter, Hashimoto, Hyperthyroid, Hypothyroid, Thyroid Dyshormonogenesis,

  • Traits - Body Odor, Personality, Behavior, Features

    • Eyes, Facial, Hair, Pigment, Strength, Talent, Taste.

  • Toxins- Detoxification ability, sensitivities, hormones, heavy metals, environmental

    • Chemicals, Diet, Industrial; Phase I detoxification, Phase II detoxification.

    • Arsenic, Cyclic Carbonates, Esters, Free Radicals, Monomethylarsonic acid, Polycyclic Aromatic Hydrocarbons, Xenobiotics.

  • Urate- Levels, Ability to breakdown/Remove, Function, Risks

    • Beta-aminoisobutyric acid, Blood urea nitrogen (BUN), Uric.

  • Vaccine- Response, Risks

    • Anthrax, Hepatitis B, Herpes, Influenza, Meningococcal, Measles, Mumps, and Rubella (MMR), Smallpox.

  • Vascular- Deficiencies, Risks/Susceptibilities

    • Endothelium dependent vasodilation, Formation, Vasodilation, Vasculitis, Volume.

    • Aortic aneurysm, Aortopathy, Atherosclerosis, Deep vein thrombosis (DVT), Ischemic stroke, Kawasaki disease, Peripheral artery disease, Small vessel occlusion, Supravalvar aortic stenosis, Vascular calcification, Venous thromboembolism.

  • Vitamins- Deficiencies, Metabolism problems (absorption), Build up

    • Molybdenum, Riboflavin- B2, Pantothenate- B5, Pyridoxine (B6), Biotin- B7, Inositol- B8, Folate- B9, B12, C, Choline, D, E, K.

  • Virus- Immunity, Risks/Susceptibilities

    • Cytomegalovirus, COVID, Swine flu (H1N1), Hepatitis B, Human papillomavirus (HPV), Herpes Simplex virus (HSV), Epstein-Barr virus (EB), Malaria, SARS.

  • Weight- Risks, Abilities, Traits, Eating behavior, Fat loss in response to exercise

    • Adiponectin, Birth, BMI, Obesity & Weight Loss Markers, Waist size.