ERBB4:Ensemblv90

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber ERBB4 in Motor Neurone Disease Level 2: Neurology and neurodevelopmental disorders Version 1.39 Component of the following Super Panels: Neurodegenerative disease - adult onset Neuromuscular Superpanel Progressive Neurological Conditions	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Victorian Clinical Genetics Services Phenotypes Amyotrophic lateral sclerosis 19 MIM#615515
Amber ERBB4 in Mendeliome Version 1.3802	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Amyotrophic lateral sclerosis 19, MIM# MIM#615515 Intellectual disability MONDO:0001071
Amber ERBB4 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Literature Phenotypes Intellectual disability Tags SV/CNV
Red ERBB4 in CGC_86 Version 0.3	0 reviews	Other	Sources CGC_86 Phenotypes NA
Amber ERBB4 in Motor Neurone Disease Level 2: Neurology and neurodevelopmental disorders Version 2.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert list Expert Review Amber Phenotypes Amyotrophic lateral sclerosis 19 MIM#615515

5 panels