CentoDx® is our largest NGS panel covering coding regions of more than 6,500 genes with known associated clinical phenotype.
CentoDx® focuses on genes for which a clear genotype phenotype correlation has been previously demonstrated in OMIM and HGMD. CentoDx® covers metabolic, neurological, reproductive, malformative, ophthalmological, oncogenetic, bone, skin, immunological, cardiovascular, nephrological, vascular, endocrine, gastrointestinal and muscoloskeletal disorders encompassing more than 3,200 rare diseases.
Why Choose CentoDx®?
High Diagnostic Accuracy With the Fastest Workflow
Why Should You Choose CentoDx®?