Myriad Women’s Health

GenCC Ref: GENCC:000108

Myriad Women’s Health

This page is a summary of pilot submissions provided by Myriad Women’s Health. Click here to be notified about GenCC updates.

As a CLIA-certified clinical testing laboratory, Myriad Women’s Health provides genetic screening and support for women and their families.


Website
Personnel
Marie Balzotti, Coordinator
Email: marie.balzotti@myriad.com

Assertion Criteria

Submissions

148 total number of submissions
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adenosine deaminase deficiency
AR
12/26/2018
Evaluated
10/13/2020
Submitted
glycogen storage disease III
AR
11/19/2018
Evaluated
10/13/2020
Submitted
primary hyperoxaluria type 1
AR
12/28/2018
Evaluated
10/13/2020
Submitted
autoimmune polyendocrine syndrome type 1
AR
08/22/2018
Evaluated
10/13/2020
Submitted
hereditary fructose intolerance
AR
06/26/2018
Evaluated
10/13/2020
Submitted
congenital disorder of glycosylation type 1C
AR
07/23/2018
Evaluated
10/13/2020
Submitted
metachromatic leukodystrophy
AR
08/17/2018
Evaluated
10/13/2020
Submitted
argininosuccinic aciduria
AR
07/25/2018
Evaluated
10/13/2020
Submitted

The GenCC database is currently released under a Fort Lauderdale Agreement for the benefit of the wider biomedical community. You can freely download and search the data, and we encourage the use and publications of validity data for specific targeted sets of genes. However, we ask that you not publish global (site-wide) analyses of these data, or of large gene sets, until after the GenCC flagship paper has been published (estimated to be spring 2022). After the flagship publication, data will be available free of restriction under a CC0 1.0 Universal (CC0 1.0) Public Domain Dedication. The GenCC requests that you give attribution to GenCC and the contributing sources whenever possible and appropriate.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. The GenCC does not independently verify the submitted information. Though the information is obtained from sources believed to be reliable, no warranty, expressed or implied, is made regarding accuracy, adequacy, completeness, reliability or usefulness of any information. This disclaimer applies to both isolated and aggregate uses of the information. The information is provided on an "as is" basis, collected through periodic submission and therefore may not represent the most up-to-date information from the submitters. If you have questions about the medical relevance of information contained on this website, please see a healthcare professional; if you have questions about specific gene-disease claims, please contact the relevant sources; and if you have questions about the representation of the data on this website, please contact gencc@thegencc.org.