Directory of Services

Multi-Gene Panels

Macrocephaly ID 156.02 Macrocephaly - basis diagnostics ID 272.01 Malignant hyperthermia susceptibility ID 76.00 Marfan syndrome - basis diagnostics ID 174.00 Maturity-onset diabetes of the young (MODY) ID 213.00 Metabolic dysmorphic syndromes ID 273.00 Metabolic myopathy - core panel, 10 genes ID 256.00 Metabolic myopathy and rhabdomyolysis, 30 genes ID 25.02 Microphthalmia-Anophthalmia-Coloboma complex (MAC) ID 119.01 Microphthalmia-Anophthalmia-Coloboma complex (MAC) - basis diagnostics ID 167.00 Mitochondrial disorders - comprehensive panel, 243 genes ID 87.03 Mitochondrial hepato(enzephalomyelo)pathy - basis diagnostics ID 264.00 Mitochondrial hepato(enzephalomyelo)pathy and phenocopies ID 53.02 Mitochondrial myopathy ID 69.02 Muscle disease with contractures and/or rigid spine ID 43.01 Muscle weakness (myopathy, muscular dystrophy) - comprehensive panel ID 89.03 Muscle weakness, adult-onset , 105 genes ID 45.02 Muscle weakness, early-onset, 128 genes ID 37.02 Muscular dystrophy, congenital merosin-deficient ID 250.00 Muscular dystrophy, congenital, 29 genes ID 251.00 Muscular dystrophy, congenital, collagen-associated (Bethlem/Ullrich and phenocopies) ID 32.01 Muscular dystrophy, congenital, collagen6-associated (Bethlem/Ullrich) ID 249.00 Muscular dystrophy, congenital, dystroglycanopathy ID 31.02 Muscular dystrophy, Emery-Dreifuss ID 22.00 Muscular dystrophy, limb-girdle - core panel ID 248.00 Muscular dystrophy, limb-girdle - non DMD associated ID 247.00 Myopathy, congenital - fetal core genes ID 294.00 Myopathy, congenital - nemaline / core / centronuclear ID 26.03 Myotonia ID 75.02 Myotonia - basis diagnostics ID 244.00