Inheritance Lab is a premier, world-class institution specializing in reproductive genetics and genomics. Founded by visionary industry leaders, the laboratory leverages over 85 years of collective expertise
in feto-maternal genetics, rare disorders, and complex prenatal and neonatal genetic diagnostics.
Rare disorders are uncommon medical conditions, often genetic, that affect a small percentage of the population and may require specialized diagnosis and care.
These tests help identify the causes of male and female infertility, detect carriers of inherited diseases, and guide antenatal planning. They also
inform the choice of assisted
reproductive techniques, optimizing the chances of successful pregnancies.
We provide advanced insights into the genetic factors driving cancer development and progression. By analyzing specific mutations and biomarkers, these tests help doctors predict therapy response, and assess inherited cancer risks.
Successfull
PGT-M cases
Premarital Diagnosis reports generated
PGT-SR reports
generated
NIPT reports
generated
(+20) 120 583 0835
(+20) 102 152 1488
(+20) 100 418 9955
Inheritance Genomic Center, El-Basatin Sharkeya, El Basatin, Cairo, Egypt, 11728
from Saturday to Thursday from
9:00 am - 4:00 pm
Now Whole Exome Sequencing Rapid Test Is Available
checking on T21, T18, T9, T16, T22, Sex chromosomes, Fetal gender, 92, and micro deletion/duplication sydromes
Combines Whole Exome Sequencing with targeted clinical insights to provide the most precise diagnosis for kidney disease available today.
a single, powerful NGS assay that analyzes hundreds of genes and cancer biomarkers simultaneously to guide personalized therapy decisions.
Beyond Exome Limits
Unlocking Genome Secrets
We now offer rapid PGT-M. This rapid test delivers results in just 3 weeks instead of a full 3 months!
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