OnlineIMD
GDAP1 deficiency
Type
Disease
External link(s)
IEMbase
Gene
GDAP1
/ Ganglioside Induced Differentiation Associated Protein 1
8q21.11
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
Ganglioside-induced differentiation-associated protein 1
Disease group(s)
19.2 Disorders of mitochondrial and peroxisomal dynamics
Child entries
Axonal Charcot-Marie-Tooth type 2K
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
Charcot-Marie-Tooth disease type 2H
Charcot-Marie-Tooth disease type 4A, demyelinating