Adult and Pediatric Patients with Concern for the Following Syndromes: 

• Hereditary cancer syndromes
• Connective tissue disorders - such as Ehlers-Danlos Syndromes or Marfan Syndrome
• Neurodevelopmental disorders - including Autism
• Hereditary amyloidosis conditions
• Movement disorders - such as Parkinson's or Huntington's disease
• Cardiomyopathy and cardiac arrhythmia syndromes
• Family history of sudden cardiac arrest
• Autoimmune and autoinflammatory syndromes
• Hereditary inflammatory bowel conditions
• Hereditary dermatologic conditions
• Endocrine disorders
• Inherited nephrology syndromes
• Congenital anomalies
• Fragile X syndrome
• Skeletal dysplasia
• Epileptic conditions
• Immunodeficiency syndromes
• Hereditary Deafness Syndromes
• Hereditary hematologic conditions
• Metabolic disorders
• Ophthalmologic conditions
• Chromosomal abnormalities
• Whole exome testing for rare or unexplained disease
• Blood testing for Active Cancer Screening
• Pharmacogenomic testing to guide medication choices - including psychiatric medications
• Carrier screening for family planning
• Family Variant testing for those with a known familial mutation