FOXR1

forkhead box R1
OMIM: 615755, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber FOXR1 in Intellectual disability Level 3: Neurodevelopmental disorders Level 2: Neurology and neurodevelopmental disorders Version 6.13 Latest signed off version: v6.0 (1 May 2024) 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

Panel

Reviews

Mode of inheritance

Details

Amber FOXR1 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0 (1 May 2024)

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