Genomics England
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Genes and Entities
SIX2
SIX homeobox 2
OMIM:
604994
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Panel
Mode of inheritance
Details
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Paediatric disorders - additional genes
Component of the following Super Panels:
- Paediatric disorders
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
six2-related frontonasal dysplasia, MONDO:0044628