Mitochondrial disorders
Gene: MTO1Comment on mode of inheritance: Confirmed on G2P and OMIM.Created: 2 Mar 2016, 12:59 p.m.
Comment on list classification: Promoted from red to green due to expert review, and it is a confirmed DD gene for infantile hypertrophic cardiomyopathy and lactic acidosis.Created: 2 Mar 2016, 12:59 p.m.
Victorian Clinical Genetics Services was added to MTO1. Panel: Mitochondrial disorders
This gene has been classified as Green List (High Evidence).
Phenotypes for MTO1 were set to Multiple respiratory chain complex deficiencies (disorders of protein synthesis); Combined oxidative phosphorylation deficiency 10, 614702; infantile hypertrophic cardiomyopathy and lactic acidosis.
Mode of inheritance for MTO1 was changed to BIALLELIC, autosomal or pseudoautosomal
This gene has been classified as Green List (High Evidence).
MTO1 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen
MTO1 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen
MTO1 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen