Endocrinology Panel
Endocrinology Panel
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The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major endocrinological conditions
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 220 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Congenital Hypothyroidism
- Aromatase Deficiency
- Congenital leptin deficiency
- Hypoplastic Pancreas-Intestinal
- Atresia-Hypoplastic Gallbladder Syndrome

This product is only meant for customers who already purchased a MyGenome Test