Genomics England
GMS Panels
Panels
Genes and Entities

WSB2

WD repeat and SOCS box containing 2
PanelMode of inheritanceDetails
1 panel
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
neurodevelopmental delay, dysmorphic features, brain structural abnormalities, growth restriction, hypotonia, microcephaly, Luo-Agrawal neurodevelopmental syndrome, OMIM:621552, neurodevelopmental disorder, MONDO:0700092