Back

CentoDx®

CUT TO THE CHASE

Exhaustive clinical information at a moderate price.
Targeting genes associated with all known clinical phenotypes - Get high diagnostic accuracy with the fastest workflow

Order a test

CentoDx®

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®?

Covers more than 6,500 clinically relevant genes with known associated phenotypes

Ideal for single gene disorders to complex phenotypes

Turnaround time of <30 business days

Comprehensive clinical report

High Diagnostic Accuracy With the Fastest Workflow

Why Should You Choose CentoDx®?

CENTOGENE PRODUCTS GENES COVERAGE
CentoXome® ~20,000

≥98%

≥20x

CentoDX®>6,500

≥98%

≥20x

NGS Panel Genomic~2-1,204 

≥99%*

≥10x

*For male samples, panels including X-chromosomal genes will reach a lower coverage of ≥97% at ≥10x.


DOWNLOADS FOR CENTODX®

Get in touch with our Partner Support

Our consultation service is available in several languages.

+49 (0) 381 - 80113 416

Mon. – Fri. 7 a.m.– 8 p.m. CET • Sat. 9 a.m – 5 p.m. CET

For our US Partners:

+1 (617) 580-2102

Mon. – Fri. 9 a.m. – 5.30 p.m. EST