Conditions | Unity Screen

Conditions

Chromosomal Conditions

22q11.2 Microdeletion Syndrome

Down Syndrome

Edwards Syndrome

Jacobs Syndrome

Klinefelter Syndrome

Patau Syndrome

Triple X Syndrome

Turner Syndrome

Recessive and X-linked Conditions

Alpha-Thalassemia

Beta-Thalassemia

Canavan Disease

Cystic Fibrosis

DMD-associated Dystrophinopathies

Familial Dysautonomia

Fragile X Syndrome

Medium-Chain acyl-CoA Dehydrogenase Deficiency (MCAD)

PMM2-Congenital Disorder of Glycosylation

Phenylalanine Hydroxylase Deficiency (PKU)

Sickle Cell Disease

Smith-Lemli-Opitz Syndrome

Spinal Muscular Atrophy

Tay-Sachs Disease

*Fetal risk assessment via cfDNA is provided via fetal sex only.