OnlineIMD
19.2 Disorders of mitochondrial and peroxisomal dynamics
Type
Group
Disease group(s)
19 Disorders of organelle biogenesis, dynamics and interactions
Child entries
Behr syndrome
Costeff syndrome
Mitofusin 2 deficiency
MSTO1 deficiency
MIEF2 deficiency
Dynamin-like protein 1 deficiency
Mitochondrial fission factor deficiency
Spartin deficiency
SPATA5 deficiency
GDAP1 deficiency
STAT2 deficiency
UGO-1 like protein deficiency
Trafficking kinesin-binding protein 1 deficiency