Full Screen – Health Conditions
- 9q22.3 microdeletion
- Ataxia-telangiectasia
- Baller-Gerold syndrome
- Bannayan-Riley-Ruvalcaba syndrome
- Beckwith-Wiedemann syndrome
- Birt-Hogg-Dube syndrome
- Bladder cancer
- Bone cancer
- Brain cancer
- Breast cancer
- Brooke-Spiegler syndrome
- Café-au-lait spots
- Cancers of the blood
- Carney complex
- Carney-Stratakis syndrome
- Cockayne syndrome
- Coffin-Siris syndrome
- Colorectal cancer
- Congenital central hypoventilation syndrome
- Congenital hyperinsulinism
- Congenital tufting enteropathy
- Core binding factor acute myeloid leukemia
- Costello syndrome
- Cowden syndrome
- Cutaneous malignant melanoma 3
- Cutaneous melanoma
- Cytogenetically normal acute myeloid leukemia
- Dendritic cell, monocyte, B lymphocyte and natural killer lymphocyte deficiency
- Denys-Drash syndrome
- Desmoid tumor
- Diabetes mellitus type 1-2
- Diabetes mellitus, insulin-dependent, 20
- DICER1 syndrome
- Familial acute myeloid leukemia with mutated CEBPA
- Familial adenomatous polyposis
- Familial cancer of breast
- Familial cylindromatosis
- Familial erythrocytosis
- Familial hemophagocytic lymphohistiocytosis
- Familial isolated acromegaly
- Familial isolated hyperparathyroidism
- Familial isolated pituitary adenoma (FIPA)
- Fanconi anemia
- Fanconi anemia complementation group B
- Fanconi anemia complementation group D2
- Fanconi anemia complementation group G
- Fanconi anemia complementation group I
- Fanconi anemia complementation group L
- Fanconi anemia complementation group M
- Fanconi anemia complementation group Q
- Fanconi anemia, complementation group E
- Fanconi anemia, complementation group F
- Fetal gigantism
- Focal cortical dysplasia of Taylor balloon cell type
- Frasier syndrome
- Fumarase deficiency
- Gastrointestinal stromal tumor
- Gorlin syndrome
- Head and neck squamous cell carcinoma
- Hepatic adenomas, familial
- Hepatocellular carcinoma
- Hereditary breast and ovarian cancer
- Hereditary diffuse gastric cancer
- Hereditary hemorrhagic telangiectasia
- Hereditary leiomyomatosis and renal cell cancer
- Hereditary multiple osteochondromas
- Hereditary parapanglioma-pheochromocytoma
- Hirschsprung disease
- Hyperparathyroidism-jaw tumor syndrome
- Immunodeficiency 21
- Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita and genital anomalies (IMAGe)
- Isolated familial somatotropinoma
- Juvenile myelomonocytic leukemia
- Juvenile polyposis syndrome
- Kidney cancer
- Langer-Giedion syndrome
- Li-Fraumeni syndrome
- Lung cancer
- Lymphangioleiomyomatosis
- Lymphedema, primary, with myelodysplasia
- Lynch syndrome
- Maturity-onset diabetes of the young, type 3
- Medulloblastoma
- Melanoma
- Mesothelioma
- Mosaic variegated aneuploidy syndrome
- Multiple endocrine neoplasia
- Multiple familial trichoepithelioma
- Myelodysplastic syndrome
- Myhre syndrome
- Neuroblastoma
- Neurofibromatosis
- Nijmegen breakage syndrome
- Nonsyndromic hearing loss
- Nonsyndromic holoprosencephaly
- Nonsyndromic paraganglioma
- Ovarian cancer
- Pancreatic cancer
- Pancreatic cancer 3
- Perlman syndrome
- Peutz-Jeghers syndrome
- Pheochromocytoma
- Piebaldism
- Potochi-Shaffer syndrome
- Premature chromatid separation trait
- Primary macronodular adrenal hyperplasia
- Primary spontaneous pneumothorax
- Prostate cancer
- Rapadilino syndrome
- Renal cell carcinoma, nonpapillary
- Renal cell carcinoma, papillary, 1
- Renal hamartomas nephroblastomatosis
- Retinoblastoma
- Rhabdoid tumor predisposition syndrome
- Rheumatoid arthritis
- Rothmund-Thomson syndrome
- Schwannomatosis
- Shwachman-Diamond syndrome
- Simpson-Golabi-Behmel syndrome
- Sotos syndrome
- Sporadic macroadenomas
- Stomach cancer
- Thyroid cancer
- Tracheoesophageal fistula
- Trichothiodystrophy
- Tuberous sclerosis complex
- Tumor predisposition syndrome
- Turcot syndrome
- Tylosis with esophageal cancer
- Type 1 diabetes
- Uterine cancer
- Uveal melanoma
- von Hippel-Lindau syndrome
- WAGR syndrome
- Weaver syndrome
- Werner syndrome
- Xeroderma pigmentosum
- Xeroderma pigmentosum complementation group E
- Xeroderma pigmentosum complementation group G
- Xeroderma pigmentosum group F
- XFE progeroid syndrome
Customer Convenience and Support
A simplified process by ordering a kit online, with easy-to-follow instructions and returning your sample in a prepaid package to our state-of-the-art lab. In addition, we offer an extensive support system to help you understand and explain the results.
Privacy control
We keep test results confidential in full compliance with HIPPA and only collect information that is needed to provide you with a high-quality experience.
Advanced technology
Innovative technologies used in products and testing include Next Generation Sequencing (NGS), qPCR, and other molecular techniques.