Search by disease or gene

LabGenetics has a disease catalog containing more than 1000 genetic tests, each of which has been optimized and validated by our professionals in our own facilities.

Depending on each of the pathologies, for the diagnosis of hereditary and/or rare diseases, LabGenetics performs different molecular studies: NGS and exomes, complete gene sequencing, analysis of frequent mutations, simultaneous sequencing of several genes, expansions, study of large deletions and duplications by MLPA, study of carriers, etc.

In addition, for all of them it is also possible to perform prenatal genetic diagnostics from uncultured fetal cells.

LabGenetics is also able to offer genetic diagnosis of hereditary and rare diseases by means of massive sequencing technology or NGS (Next Generation Sequencing).