Genomics England
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Genes and Entities
KCTD17
potassium channel tetramerization domain containing 17
OMIM:
616386
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Panel
Mode of inheritance
Details
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Childhood onset dystonia, chorea or related movement disorder
R-numbers:
R57
Signed-off version 4.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Dystonia 26, myoclonic