FOXR1

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber FOXR1 in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Literature Phenotypes Postnatal microcephaly, progressive brain atrophy and global developmental delay
Amber FOXR1 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.269	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Literature Phenotypes Postnatal microcephaly, progressive brain atrophy and global developmental delay
Amber FOXR1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Literature Phenotypes Postnatal microcephaly, progressive brain atrophy and global developmental delay
Red FOXR1 in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Postnatal microcephaly, progressive brain atrophy and global developmental delay

4 panels