NDUFC2

Panel	Reviews	Mode of inheritance	Details
Amber NDUFC2 in Mendeliome Version 1.2302	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Mitochondrial complex I deficiency, nuclear type 36, MIM# 619170
Amber NDUFC2 in Mitochondrial disease Level 2: Metabolic disorders Version 0.969 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Mitochondrial complex I deficiency, nuclear type 36, MIM# 619170

Panel

Reviews

Mode of inheritance

Details

Version 1.2302

1 review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Metabolic disorders
Version 0.969

Component of the following Super Panels:

Metabolic Disorders Superpanel

Progressive Neurological Conditions

1 review

BIALLELIC, autosomal or pseudoautosomal

2 panels