Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency

Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency (disorder)

active

Code	`771478008`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20190131

Synonyms

COXPD10 - combined oxidative phosphorylation defect type 10
Combined oxidative phosphorylation defect type 10
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimisation 1 deficiency
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency

Parents (6)

85995004Autosomal recessive hereditary disorder disorder
363005004Cardiovascular system hereditary disorder disorder
762228008Congenital cardiovascular disorder disorder
237987001Deficiency in enzyme complexes of mitochondrial respiratory chain disorder
472316006Hypertrophic mitochondrial cardiomyopathy disorder
240096000Mitochondrial cytopathy disorder

Children (0)

None (leaf concept).