Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Mitochondrial disease
/
Inborn mitochondrial metabolism disorder
/
Mitochondrial oxidative phosphorylation disorder
/
Combined oxidative phosphorylation deficiency
Combined oxidative phosphorylation deficiency 60
rare
Identifiers
MONDO:0978298
OMIM:621195
Causal genes
MRPL49
Part of
Combined oxidative phosphorylation deficiency
Projects
Sign in to start a project
No projects yet.