RRM1

ribonucleotide reductase catalytic subunit M1
OMIM: 180410, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red RRM1 in DDG2P Version 4.3 Latest signed off version: v4.0 (1 May 2024) Component of the following Super Panels: Paediatric disorders	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red DD-Gene2Phenotype Phenotypes RRM1-related mitochondrial DNA depletion/deletions syndrome

Panel

Reviews

Mode of inheritance

Details

Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

Paediatric disorders

review

BOTH monoallelic and biallelic, autosomal or pseudoautosomal