Genomics England
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Genes and Entities
FITM2
fat storage inducing transmembrane protein 2
OMIM:
612029
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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 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Siddiqi syndrome OMIM:618635, siddiqi syndrome MONDO:0032842