F-box and leucine rich repeat protein 3
OMIM: 605653
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Short stature, Intellectual developmental disorder with short stature, facial anomalies, and speech defects, 606220, Intellectual disability