This panel is used for clinical indication 'R333 Central congenital hypoventilation' in the NHS Genomic Medicine Service. Further information on the testing criteria and any overlapping clinical indications can be found within (https://www.england.nhs.uk/publication/national-genomic-test-directories/) under 'R333 Central congenital hypoventilation'. This panel will continue to be curated based on external reviews and Genomics England curation. New changes will be reflected in an increase to the minor version of the panel and details of these can be viewed in the 'Panel Activity' page. Periodically, these changes will be reviewed by a NHS Genomic Medicine Service evaluation process. The content that is agreed for the GMS panels will be reflected in an updated version number. CNVs, STRs and genes encoded by the mitochondrial genome may not be routinely included in the analysis where the panel is NOT delivered by WGS. Please contact your Genomic Laboratory Hub for information regarding specific queries.
Ian Berry (Leeds Genetics Laboratory)
Group: Other NHS organisation
Workplace: NHS diagnostic lab
Achchuthan Shanmugasundram (Genomics England Curator)
Group: Other
Workplace: Other
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2 Entitiess
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PHOX2B |
1 review1 green |
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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Phenotypes
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LBX1 |
2 reviews1 green |
BIALLELIC, autosomal or pseudoautosomal |
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Phenotypes
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2023-09-14 13:14 Achchuthan Shanmugasundram (Genomics England Curator) promoted panel to 1.0
The content of this panel has been produced in agreement with the NHS Genomic Medicine Service. The panel was promoted to the first major version (1.0) following this.