Genes cure Tests
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Genes Tests
Lynch Syndrome Testing (for colorectal cancer risk)
What is Lynch Syndrome Testing? Lynch syndrome is a hereditary condition that increases the risk of developing certain types of…
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Genes Tests
BRCA1/BRCA2 Testing (for breast and ovarian cancer risk)
What is BRCA1/BRCA2 Testing? BRCA1 and BRCA2 are genes that help repair damaged DNA. Mutations in these genes can significantly…
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Genes Tests
Methylmalonic Acidemia (MMA) Screening
What is Methylmalonic Acidemia (MMA) Screening? Methylmalonic acidemia (MMA) is a rare genetic disorder that affects the body’s ability to…
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Genes Tests
Tyrosinemia Type I Screening
Tyrosinemia Type I is a rare genetic disorder that affects the liver’s ability to break down tyrosine, an amino acid.…
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Genes Tests
Homocystinuria Screening
What is Homocystinuria Screening? Homocystinuria screening is a genetic test to detect a rare metabolic disorder called homocystinuria. This condition…
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Genes Tests
Biotinidase Deficiency Screening
What is Biotinidase Deficiency Screening ? Biotinidase deficiency screening is a newborn screening test that checks for a rare genetic…
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Genes Tests
Maple Syrup Urine Disease (MSUD) Screening
What is Maple Syrup Urine Disease (MSUD) Screening? Maple Syrup Urine Disease (MSUD) is a rare genetic disorder that affects…
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Genes Tests
Cystic Fibrosis Screening
What is Cystic Fibrosis Screening? Cystic Fibrosis (CF) screening is a genetic test used to identify carriers of the CF…
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Genes Tests
Sickle Cell Disease Screening
What is Sickle Cell Disease Screening? Sickle Cell Disease (SCD) screening is a genetic test to determine if a person…
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Genes Tests
Galactosemia Screening
What is Galactosemia Screening ? Galactosemia screening is a newborn screening test that checks for a rare genetic disorder called…
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