Genomics England
GMS Panels
Panels
Genes and Entities
FOXI3
forkhead box I3
OMIM:
612351
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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, imprinted status unknown
Phenotypes
Bilateral Microtia, Congenital aural atresia