Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Mitochondrial disease
/
Inborn mitochondrial metabolism disorder
/
Mitochondrial oxidative phosphorylation disorder
FASTKD2-related infantile mitochondrial encephalomyopathy
rare
Identifiers
MONDO:0015632
Orphanet:166105
Part of
Mitochondrial oxidative phosphorylation disorder
Projects
Sign in to start a project
No projects yet.