FOXR1

forkhead box R1
OMIM: 615755, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FOXR1 in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.544
Latest signed off version: v5.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Global developmental delay, HP:0001263
    • microcephaly, MONDO:0001149
    • Brain atrophy, HP:0012444