Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
Cowden syndrome 1
Lhermitte-Duclos disease
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
10/31/2023
PubMed IDs:
10400993 10910075 11755638 12928488 12938083 15254063 15589575 17392703 17768394 18972196 19847259 20565722 21194675 21303970 21430697 21659347 22252256 23335809 23934601 24136893 26678657 26798346 27890237 28526761 30287823 31216739 32923874 8673088 9345101 9467011
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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.