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
/
Mitochondrial respiratory chain complex deficiency
/
Mitochondrial complex IV deficiency, nuclear-type
Mitochondrial complex IV deficiency, nuclear type 24
rare
Identifiers
MONDO:0980755
OMIM:621431
Causal genes
FASTKD5
Part of
Mitochondrial complex IV deficiency, nuclear-type
Projects
Sign in to start a project
No projects yet.