ROBO1

roundabout guidance receptor 1
OMIM: 602430
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 3.122
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
tetralogy of Fallot and septal defects
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.343
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intellectual disability, MONDO:0001071, Neurooculorenal syndrome, OMIM:620305