SLC25A21

solute carrier family 25 member 21
OMIM: 607571, Gene2Phenotype

2 panels

Panel	Reviews	Mode of inheritance	Details
Amber SLC25A21 in Mendeliome Version 1.2302	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber NHS GMS Phenotypes Mitochondrial DNA depletion syndrome-18, MIM#618811
Amber SLC25A21 in Mitochondrial disease Level 2: Metabolic disorders Version 0.969 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber NHS GMS Expert Review Amber NHS GMS Phenotypes Mitochondrial DNA depletion syndrome-18 MIM#618811

Panel

Reviews

Mode of inheritance

Details

Version 1.2302

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Metabolic disorders
Version 0.969

Component of the following Super Panels:

Metabolic Disorders Superpanel

Progressive Neurological Conditions

review

BIALLELIC, autosomal or pseudoautosomal