3-methylcrotonyl-CoA carboxylase deficiency
-A-
Abdominal aneurysm
Age-related macular degeneration
Alpha-1 antitrypsin deficiency
Alzheimer’s disease, late onset
Amyotrophic lateral sclerosis
Asthma
Atrial fibrillation
- B -
Beta thalassemia
Biotinidase deficiency
Bloom syndrome
Brain aneurysm
Breast cancer
- C -
Canavan disease
Colorectal cancer
Coronary artery disease
Crohn’s disease
Cystic Fibrosis
- D -
Deep vein thrombosis
Diabetes, Type 1
Diabetes, Type 2
- F -
Factor XI deficiency
Familial dysautonomia
Familial Mediterranean fever
Fanconi anemia
- G -
Galactosemia
Gaucher disease
Glaucoma
Glutaric acidemia I
Glycogen storage disease type Ia
- H -
Hearing loss, nonsyndromic
Heart attack
Hemochromatosis
Hemoglobin C diseases
Hemoglobin E diseases
HMG-CoA lyase deficiency
Hypertension
- L -
Lactose intolerance
Leukemia, chronic lymphocytic
Lung cancer
Lupus
- M -
Macular degeneration
Maple syrup urine disease
Medium-chain acyl-coA dehydrogenase deficiency
Melanoma
Methylmalonic acidemia
Mucolipidosis type IV
Multiple carboxylase deficiency
Multiple sclerosis
Myocardial infarction
- N -
Niemann-Pick disease
- O -
Obesity
Osteoarthritis
- P -
Parkinson’s disease
Peripheral arterial disease
Phenylketonuria
Polycystic kidney disease
Pompe disease
Propionic acidemia
Prostate cancer
Psoriasis
- R -
Restless legs syndrome
Rheumatoid arthritis
- S -
Sick sinus syndrome
Sarcoidosis
Stomach cancer, diffuse
- T -
Tay-Sachs disease
Tay-Sachs pseudodeficiency
Tyrosinemia type I
- U -
Ulcerative colitis
- V -
Very long-chain acyl-coA dehydrogenase deficiency
Carrier Status:
· 3-methylcrotonyl-CoA carboxylase deficiency
· Alpha-1 antitrypsin deficiency
· Amyotrophic lateral sclerosis
· Beta thalassemia
· Biotinidase deficiency
· Bloom syndrome
· Canavan disease
· Cystic Fibrosis
· Diabetes, permanent neonatal
· Factor XI deficiency
· Familial dysautonomia
· Familial Mediterranean fever
· Fanconi anemia
· Galactosemia
· Gaucher disease
· Glutaric acidemia I
· Glycogen storage disease type Ia
· Hearing loss, nonsyndromic
· Hemochromatosis
· Hemoglobin C diseases
· Hemoglobin E diseases
· HMG-CoA lyase deficiency
· Maple syrup urine disease
· Medium-chain acyl-coA dehydrogenase deficiency
· Methylmalonic acidemia
· Mucolipidosis type IV
· Multiple carboxylase deficiency
· Niemann-Pick disease
· Phenylketonuria
· Polycystic kidney disease
· Pompe disease
· Propionic acidemia
· Sick sinus syndrome
· Tay-Sachs disease
· Tay-Sachs pseudodeficiency
· Tyrosinemia type I
· Very long-chain acyl-coA dehydrogenase deficiency
Drug Response/Metabolism Test:
· Abacavir Hypersensitivity
· Caffeine Metabolism
· Carbamazepine Hypersensitivity
· Clopidrogel Metabolism
· Methotrexate Toxicity
· Statin Induced Myopathy
· Statin protection against myocardial infarction
· Tamoxifen Response
· Warfarin Metabolism
Ancestry Test:
· Haplotype group matching
Metabolic Health Assessment:
· Cardiac health
· Diabetes type II and Obesity
· Immune Efficiency
Vision Genetics:
· Glaucoma
· Macular Degeneration
· Age-related Macular Degeneration
Athletic Performance:
· Ability to customize training programs to optimize performance based on your genetic makeup
· Reduce risk of personal injury
· Understand nutritional requirements that are relevant specifically to you and your personal DNA
· Identify sports related activities your genetics can help you excel in
· Identify sports activities to avoid
Paternity Test – Legal and Non legal
Allergy Test:
· Pollens
· Timothy Grass
· Bermuda Grass
· Mountain Cedar (Juniper)
· Short Ragweed
· Milk
· Egg White
· Wheat
Mold Other· Alternaria
· Cat
· House Dust Mite*Represents approximately 90% of all common human allergies
Hair Drug Test:
• cocaine products and derivatives • opiates and codeine derivatives (oxycontin etc.) • amphetamine ans derivatives • marijuana/hashish (THC) • phencyclidine
90 day history
Saliva Drug:
1-72 hour history
· Amphetamines
· Benzodiazepines
· Cocaine
· Morphine
· Marijuana
Dog Breed Testing
OTHER TESTS:
Celiac Disease Testing
- 10 minute diagnostic blood testingMenopause Test Kit
- Urinalysis