FOXR1

forkhead box R1
OMIM: 615755, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FOXR1 in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

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