OnlineIMD
Mitofusin 2 deficiency
Type
Disease
External link(s)
Orphanet
IEMbase
Gene
MFN2
/ Mitofusin 2
1p36.22
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
Mitofusin-2
Disease group(s)
19.2 Disorders of mitochondrial and peroxisomal dynamics
Child entries
Axonal Charcot-Marie-Tooth type 2A2
Hereditary motor and sensory neuropathy type 5
Multiple symmetric lipomatosis