CENTOGENE’s pediatric portfolio supports the diagnosis of early and childhood-onset disorders through comprehensive genetic testing across 14 disease areas.
Combining pediatric-focused curation, advanced genomic technologies, and deep scientific expertise, the portfolio enables earlier and more informed diagnoses across a broad spectrum of pediatric conditions. Dedicated disease-focused sub-panels and genome-based analysis support the detection of complex variants while enabling confident variant interpretation and informed clinical decision-making.
14
Pediatric disease areas
+1 Million
Patient cases in the CENTOGENE biodatabank
>43
Curated diagnostic genes
Whole Genome Sequencing (WGS), offers the most comprehensive one-step solution with the highest diagnostic yield
Whole Exome Sequencing (WES) enables quicker and cost-effective diagnosis for patients with complex and unclear symptoms
Multiomics give a deeper understanding of human biological processes and acts as a unique and highly effective tool for early diagnosis
Create a diagnostic gene panel by selecting genes tailored to individual patient needs.
2 to >4.000
Selectable Genes
15 Business Days
TAT
Genome or Exome
Backbone
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