Disease #00488

Official abbreviation	CMT2A2
Name	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2
OMIM ID	609260
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MFN2
Associated tissues	-
Disease features	-
Remarks	-