FBXO22

F-box protein 22
OMIM: 609096
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 10.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Tayoun-Maawali syndrome, OMIM:621184
R-numbers: R453
Signed-off version 2.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Tayoun-Maawali syndrome, OMIM:621184