ERMARD

ER membrane associated RNA degradation
OMIM: 615532, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red ERMARD in Periventricular Grey Matter Heterotopia Level 2: Neurology and neurodevelopmental disorders Version 1.2 Component of the following Super Panels: Malformations of cortical development_Superpanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Australian Genomics Health Alliance Brain Malformation Flagship Victorian Clinical Genetics Services Phenotypes Periventricular nodular heterotopia 6, MIM#615544
Red ERMARD in Mendeliome Version 1.1902	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Periventricular nodular heterotopia 6, MIM#615544
Red ERMARD in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.522	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Australian Genomics Health Alliance Brain Malformation Flagship Victorian Clinical Genetics Services Phenotypes Periventricular nodular heterotopia 6, MIM#615544
Red ERMARD in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Genetic Health Queensland Phenotypes Periventricular nodular heterotopia 6, MIM#615544
Red ERMARD in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes Periventricular nodular heterotopia 6 (MIM#615544)