FBXW11

F-box and WD repeat domain containing 11
OMIM: 605651
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
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