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
/
Inherited lipoic acid biosynthesis defect
/
Fatal multiple mitochondrial dysfunctions syndrome
Multiple mitochondrial dysfunctions syndrome 5
rare
Identifiers
MONDO:0033282
OMIM:617613
Orphanet:569274
Causal genes
ISCA1
Part of
Fatal multiple mitochondrial dysfunctions syndrome
Also known as
MMDS5
Projects
Sign in to start a project
No projects yet.