Genomics Services
Hereditary diseases are the genetic disorder that are passed on from one generation to another through defective genes. In certain conditions the disease symptoms are not observed but the defective gene is present in body, these humans are carriers of disease. If both the partners have family histories of disease they can pass the defective genes to their next generation which cause disease in children. Hereditary disease test identifies genetic mutation gives information regarding their offspring's potential health risk.
Test Offered
Beta Thalassemia

Sickle Cell Anemia

MTHFR (Methylenetetrahydrofolate reductase)

Lactose Intolerance

Cystic Fibrosis (CFTR Mutation)

Biotinidase Deficiency

Hereditary Hemochromatosis
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