OnlineIMD
Dynamin 2 deficiency
Type
Disease
External link(s)
IEMbase
Gene
DNM2
/ Dynamin 2
19p13.2
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
Dynamin-2
Disease group(s)
23.6 Disorders of the synaptic vesicle cycle
Child entries
Autosomal dominant centronuclear myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Fetal akinesia-cerebral and retinal hemorrhage syndrome