FBXO31

F-box protein 31
OMIM: 609102
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
?Mental retardation, autosomal recessive 45, OMIM:615979, Intellectual disability, autosomal dominant