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 52
rare
Identifiers
MONDO:0030311
OMIM:619386
Causal genes
NFS1
Part of
Combined oxidative phosphorylation deficiency
Also known as
COXPD52
Projects
Sign in to start a project
No projects yet.