FMN2

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green FMN2 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Intellectual developmental disorder, autosomal recessive 47, MIM#616193
Green FMN2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Intellectual developmental disorder, autosomal recessive 47, MIM#616193
Red FMN2 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Phenotypes Intellectual developmental disorder, autosomal recessive 47, MIM#616193

3 panels