Term Name:	Charcot-Marie-Tooth disease, axonal type 2W
Synonyms:	autosomal dominant axonal Charcot-Marie-Tooth disease type 2W, Charcot-Marie-Tooth neuropathy type 2W, CMT2W
Definition:	A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31.
Ontology:	Human Disease [DOID:0110162]   ( DOID:0110162 )