Genomics England
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Genes and Entities
PDE2A
phosphodiesterase 2A
OMIM:
602658
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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
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
infantile‐onset chorea‐predominant movement disorder