MRPL39

Panel	Reviews	Mode of inheritance	Details
Green MRPL39 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Combined oxidative phosphorylation deficiency-59 (COXPD59), MIM#620646
Green MRPL39 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 Literature Phenotypes Combined oxidative phosphorylation deficiency-59 (COXPD59), MIM#620646

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

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