Category: CVS

RETT Syndrome

Cystic Fibrosis – 34 mutations

Hemochromatosis – 3 Mutations

Rare Hereditary Hemochromatosis Type 4

Hemochromatosis – 12 Mutations

Hemochromatosis – 18 Mutations

Spinocerebellar Ataxia Type 3

Tay Sachs (HEXA) Disease – Most Mutations

Hereditary Spastic Paraplegia – Panel

Hereditary Deafness – GJB6/CX30 Gene Sequencing