Genomics England
GMS Panels
Panels
Genes and Entities

FBXW11

F-box and WD repeat domain containing 11
OMIM: 605651
PanelMode of inheritanceDetails
1 panel
Green
in Intellectual disability - microarray and sequencing
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Global developmental delay, Intellectual disability, Abnormality of the eye, Abnormality of the head, Abnormality of digit, Neurodevelopmental, jaw, eye, and digital syndrome MIM#618914