USMG5

Panel	Reviews	Mode of inheritance	Details
Amber USMG5 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6 MIM#618683
Amber USMG5 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 Amber NHS GMS Phenotypes Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6 MIM#618683

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