Myriad Women’s Health

GenCC Ref: GENCC:000108

Myriad Women’s Health

This page is a summary of 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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severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to 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
ALG6-congenital disorder of glycosylation 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 data are 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 accepted Flagship manuscript is now available from Genetics in Medicine (https://www.gimjournal.org/article/S1098-3600(22)00746-8/fulltext).

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.