QRSL1

Panel	Reviews	Mode of inheritance	Details
Green QRSL1 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Combined oxidative phosphorylation deficiency 40
Green QRSL1 in Mitochondrial disease Level 2: Metabolic disorders Version 0.927 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Australian Genomics Health Alliance Mitochondrial Flagship Phenotypes Combined oxidative phosphorylation deficiency 40

Panel

Reviews

Mode of inheritance

Details

Version 1.1891

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Metabolic disorders
Version 0.927

Component of the following Super Panels:

Metabolic Disorders Superpanel

Progressive Neurological Conditions

review

BIALLELIC, autosomal or pseudoautosomal

2 panels