Genomics England
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Panels
Genes and Entities
SEMA6B
semaphorin 6B
OMIM:
608873
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Panel
Mode of inheritance
Details
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in
Genetic epilepsy syndromes
R-numbers:
R59
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Epilepsy, progressive myoclonic, 11 OMIM:618876